Benzazolonylcarbonylcyclohexenones and their use as herbicides

ABSTRACT

Cyclohexenone derivatives of benzazolones of the formula I 
                 
 
where the variables R 1 , R 2 , R 3 , A and Hex are as defined in claim  1 , and their salts, and their use for controlling harmful plants, are described.

The present invention relates to cycloyexenone derivatives of benzazolones (benzazolonylcarbonylcyclohexenones), to compositions comprising such compounds, and to the use of the cyclohexenone derivatives or of the compositions comprising them for controlling harmful plants. Moreover, the invention relates to benzazolonecarboxylic acids, which are important intermediates for preparing such cyclohexenone derivatives.

EP-A 283 261 discloses cyclohexane-1,3-diones in which the cyclohexenone ring in the 2-position is substituted by a heteroaromatic radical which is attached via a carbonyl group. Heteroaromatic radicals mentioned are sulfur-, nitrogen- and/or oxygen-containing 5-membered or 6-membered heterocycles.

WO 96/05182 discloses saccharin derivatives which have herbicidal action and are substituted on the benzene ring of the saccharin skeleton by a (2-cyclohexane-1,3-dione)carbonyl radical.

WO 97/09324 discloses cyclohexane-1,3-diones which have herbicidal action and, in the 2-position, a benzo-fused sulfur heterocycle, for example a thiochromane or a benzodihydrothiophene radical, which is attached via a carbonyl group.

WO 00/20408 describes inter alia herbicides based on cyclohexenone derivatives of the formula (a)

in which R is a methylene group, X is a hydrogen atom, a halogen atom or the like, G is a 3- to 5-membered chain which, together with the two carbons of the benzene ring to which G is attached, forms a 5- to 7-membered saturated or unsaturated fused ring, Z¹ is a halogen atom or the like, m is an integer from zero to four and q is either one or two.

PCT/EP 00/04042 discloses benzoheterocyclylcyclohexenones. Heterocyclic radicals mentioned are, inter alia, benzoxazolyl, benzimidazolyl, benzothiazolyl and benzotriazinyl. The compounds have herbicidal action.

However, the herbicidal properties of the compounds known from the publications mentioned and their compatibility with crop plants do not meet all of the criteria required from herbicides.

It is an object of the present invention to provide novel compounds having herbicidal action which preferably have greater activity than the herbicidal substances of the prior art and/or better selectivity for harmful plants.

We have found that this object is achieved by cyclohexenone derivatives of benzazolones of the formula I defined below.

Consequently, the present invention relates to cyclohexenone derivatives of benzo-fused, unsaturated 5-membered nitrogen heterocycles of the formula I

in which A, R¹, R², R³ and Hex are as defined below:

-   A is O, S, SO, SO₂ or NR⁶;     -   R¹ is halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-hydroxyalkyl,         C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-haloalkoxy-C₁-C₄-alkyl,         C₁-C₄-haloalkylthio-C₁-C₄-alkyl, C₁-C₄-alkylthio-C₁-C₄-alkyl,         C₁-C₄-alkylsulfonyl-C₁-C₄-alkyl,         C₁-C₄-haloalkylsulfonyl-C₁-C₄-alkyl, C₁-C₄-alkoxy,         C₁-C₄-hydroxyalkoxy, C₁-C₄-haloalkoxy,         C₁-C₄-alkoxy-C₁-C₄-alkoxy, C₁-C₄-haloalkoxy-C₁-C₄-alkoxy,         C₁-C₄-alkylthio, C₁-C₄-haloalkylthio, C₁-C₄-alkylsulfonyl,         C₁-C₄-haloalkylsulfonyl;     -   R² is hydrogen, hydroxyl, nitro, amino, C₁-C₆-alkylamino,         di(C₁-C₆-alkyl)amino, cyano, CHO, C₁-C₆-alkoxy, C₁-C₆-alkyl,         C₁-C₆-hydroxyalkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl,         C₁-C₆-haloalkoxy-C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl,         C₁-C₆-haloalkoxy-C₂-C₆-alkenyl, C₁-C₆-alkoxy-C₂-C₆-alkenyl,         C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,         C₁-C₆-haloalkoxy-C₂-C₆-alkynyl, C₁-C₆-alkoxy-C₂-C₆-alkynyl,         C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl,         (C₁-C₆-alkyl)carbonyl, C₁-C₆-haloalkylcarbonyl,         hydroxycarbonyl-C₁-C₄-alkyl, C₁-C₆-alkoxycarbonyl-C₁-C₆-alkyl, a         radical of the formula C(O)OR⁴, CON(R⁵)₂ or C(═NOR^(4a))R^(4b),         aryl, aryl-C₁-C₄-alkyl, arylsulfonyl, arylcarbonyl,         C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl, 3-, 4-, 5-, 6- or         7-membered heterocyclyl, 3-, 4-, 5-, 6- or 7-membered         heterocyclyl-C₁-C₆-alkyl, where each aryl, cycloalkyl,         cycloalkenyl and each heterocyclyl radical may be unsubstituted         or may carry one, two, three or four substituents, in each case         se lected from the group consisting of halogen, C₁-C₄-haloalkyl,         C₁-C₄-alkoxy and C₁-C₄-haloalkoxy;     -   R³ is hydrogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl,         C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-haloalkoxy-C₁-C₄-alkyl or         halogen;         in which     -   R⁴ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl,         C₁-C₆-haloalkoxy-C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl,         C₁-C₆-haloalkoxy-C₂-C₆-alkenyl, C₁-C₆-alkoxy-C₂-C₆-alkenyl,         C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,         C₁-C₆-haloalkoxy-C₂-C₆-alkynyl, C₁-C₆-alkoxy-C₂-C₆-alkynyl;     -   R^(4a), R^(4b) independently of one another may have the         meanings mentioned for R⁴, and R^(4b) may be hydrogen;     -   R⁵ independently of one another are hydrogen, C₁-C₆-alkyl,         C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl,         (C₁-C₆-haloalkoxy)-C₁-C₆-alkyl, C₂-C₆-alkenyl,         C₂-C₆-haloalkenyl, C₁-C₆-haloalkyl-C₂-C₆-alkenyl,         C₁-C₆-haloalkoxy-C₂-C₆-alkenyl, C₁-C₆-alkoxy-C₂-C₆-alkenyl,         C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₁-C₆-haloalkyl-C₂-C₆-alkynyl,         C₁-C₆-haloalkoxy-C₂-C₆-alkynyl, C₁-C₆-alkoxy-C₂-C₆-alkynyl, or         together form a 3- to 7-membered heterocycle which may be         partially or fully halogenated and/or may carry one, two or         three substituents selected from the group consisting of         C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy;     -   R⁶ is hydrogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl,         C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl; and     -   Hex is substituted (3-oxo-1-cyclohexen-2-yl)carbonyl of the         formula IIa or substituted (1,3-dioxo-2-cyclohexyl)methylidene         of the formula IIb         in which the variables R⁷ to R¹³ are as defined below:     -   R⁷ is hydroxyl, mercapto, halogen, OR¹⁴, SR¹⁴, SOR¹⁵, SO₂R¹⁵,         OSO₂R⁵, P(O)R¹⁶R¹⁷, OP(O)R¹⁶R¹⁷, P(S)R¹⁶R¹⁷, OP(S)R¹⁶R¹⁷,         NR¹⁸R¹⁹, ONR¹⁸R¹⁹ or N-bonded heterocyclyl which may be         partially or fully halogenated and/or may carry one to three of         the following radicals: nitro, cyano, C₁-C₄-alkyl,         C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;     -   R⁸, R¹² independently of one another are hydrogen, C₁-C₄-alkyl         or C₁-C₄-alkoxycarbonyl;     -   R⁹, R¹¹, R¹³ independently of one another are hydrogen or         C₁-C₄-alkyl;     -   R¹⁰ is hydrogen, halogen, hydroxyl, C₁-C₆-alkyl,         C₁-C₆-haloalkyl, di-(C₁-C₆-alkoxy)-methyl,         (C₁-C₆-alkoxy)-(C₁-C₆-alkylthio)methyl,         di-(C₁-C₆-alkylthio)methyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy,         C₁-C₆-alkylthio, C₁-C₆-haloalkylthio, C₁-C₆-alkylsulfinyl,         C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl,         C₁-C₆-haloalkylsulfonyl, C₁-C₆-alkoxycarbonyl,         C₁-C₆-halogenalkoxycarbonyl;     -    is 1,3-dioxolan-2-yl, 1,3-dioxan-2-yl, 1,3-oxathiolan-2-yl,         1,3-oxathian-2-yl, 1,3-dithiolan-2-yl or 1,3-dithian-2-yl, where         the six lastmentioned radicals may be substituted by one to         three C₁-C₄-alkyl radicals;         or     -   R⁹ and R¹¹ or R¹¹and R¹³ together form a π bond or a         C₁-C₅-alkylene chain which may carry one, two or three radicals         from the following group: halogen, cyano, C₁-C₄-alkyl,         C₁-C₄-haloalkyl or C₁-C₄-alkoxycarbonyl;         or     -   R⁹ and R¹³ together form a C₁-C₄-alkyl chain which may carry         one, two or three radicals from the following group: halogen,         cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl or C₁-C₄-alkoxycarbonyl;         or     -   R¹⁰ and R¹¹ together form a —O—(CH₂)_(p)—O—, —O—(CH₂)_(p)—S—,         —S—(CH₂)_(p)—S—, —O—(CH₂)_(q)— or —S—(CH₂)_(q)— chain, in which         p is 2, 3, 4 or 5 and q is 2, 3, 4, 5 or 6, which may be         substituted by one, two or three radicals from the following         group: halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl or         C₁-C₄-alkoxycarbonyl;         or     -   R¹⁰ and R¹¹, together with the carbon to which they are         attached, form a carbonyl group;         where     -   R¹⁴ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl,         C₃-C₆-alkynyl, C₃-C₆-haloalkynyl, C₃-C₆-cycloalkyl,         C₁-C₆-alkylcarbonyl, C₂-C₆-alkenylcarbonyl,         C₂-C₆-alkynylcarbonyl, C₃-C₆-cycloalkylcarbonyl,         C₁-C₆-alkoxycarbonyl, C₃-C₆-alkenyloxycarbonyl,         C₃-C₆-alkynyloxycarbonyl, C₁-C₆-alkylthiocarbonyl,         C₁-C₆-alkylaminocarbonyl, C₃-C₆-alkenylaminocarbonyl,         C₃-C₆-alkynylaminocarbonyl, N,N-di(C₁-C₆-alkyl)aminocarbonyl,         N-(C₃-C₆-alkenyl)-N-(C₁-C₆-alkyl)aminocarbonyl,         N-(C₃-C₆-alkynyl)-N-(C₁-C₆-alkyl)amino-carbonyl,         N-(C₁-C₆-alkoxy)-N-(C₁-C₆-alkyl)aminocarbonyl,         N-(C₃-C₆alkenyl)-N-(C₁-C₆-alkoxy)aminocarbonyl,         N-(C₃-C₆-alkynyl)-N-(C₁-C₆-alkoxy)aminocarbonyl,         di(C₁-C₆-alkyl)aminothiocarbonyl, C₁-C₆-alkoxyimino-C₁-C₆-alkyl,         where the alkyl, cycloalkyl or alkoxy radicals mentioned may be         partially or fully halogenated and/or may carry one, two or         three of the following groups: cyano, C₁-C₄-alkoxy,         C₁-C₄-alkylthio, di(C₁-C₄-alkyl)amino, C₁-C₄-alkylcarbonyl,         C₁-C₄-alkoxycarbonyl, C₁-C₄-alkoxy-C₁-C₄-alkoxycarbonyl,         hydroxycarbonyl, C₁-C₄-alkylaminocarbonyl,         di(C₁-C₄-alkyl)-aminocarbonyl, aminocarbonyl,         C₁-C₄-alkylcarbonyloxy or C₃-C₆-cycloalkyl;     -    is phenyl, phenyl-C₁-C₆-alkyl, phenylcarbonyl-C₁-C₆-alkyl,         phenylcarbonyl, phenoxycarbonyl, phenyloxythiocarbonyl,         phenylaminocarbonyl, N-(C₁-C₆-alkyl)-N-phenylaminocarbonyl,         phenyl-C₂-C₆-alkenylcarbonyl, heterocyclyl,         heterocyclyl-C₁-C₆-alkyl, heterocyclylcarbonyl-C₁-C₆-alkyl,         heterocyclylcarbonyl, heterocyclyloxycarbonyl,         heterocyclyloxythiocarbonyl, heterocyclylaminocarbonyl,         N-(C₁-C₆-alkyl)-N-heterocyclylaminocarbonyl, or         heterocyclyl-C₁-C₆-alkenylcarbonyl, where the phenyl and the         heterocyclyl radical of the 18 lastmentioned substituents may be         partially or fully halogenated and/or may carry one to three of         the following radicals: nitro, cyano, C₁-C₄-alkyl,         C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;     -   R¹⁵ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-alkynyl or         C₃-C₆-cycloalkyl, where the four radicals mentioned. may be         partially or fully halogenated and/or may carry one, two or         three of the following groups: cyano, C₁-C₄-alkoxy,         C₁-C₄-haloalkoxy, C₁-C₄-alkylthio, C₁-C₄-haloalkylthio,         C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl or         C₁-C₄-haloalkoxycarbonyl;     -    is phenyl, phenyl-C₁-C₄-alkyl, heterocyclyl or         heterocyclyl-C₁-C₄-alkyl, where the phenyl and the heterocyclyl         radical of the four lastmentioned substituents may be partially         or fully halogenated and/or may carry one, two or three of the         following radicals: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl,         C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl;     -   R¹⁶, R¹⁷ independently of one another are hydrogen, hydroxyl,         C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-alkylthio, phenyl,         phenyl-C₁-C₄-alkyl or phenoxy, where the three lastmentioned         substituents may be partially or fully halogenated and/or may         carry one, two or three of the following radicals: nitro, cyano,         C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or         C₁-C₄-alkoxycarbonyl;     -   R¹⁸ is hydrogen, C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl,         C₃-C₆-alkynyl, C₃-C₆-haloalkynyl, C₃-C₆-cycloalkyl,         C₁-C₆-alkylcarbonyl, hydroxyl, C₁-C₆-alkoxy, C₃-C₆-alkenyloxy,         C₃-C₆-alkynyloxy, amino, C₁-C₆-alkylamino, di(C₁-C₆-alkyl)amino         or C₁-C₆-alkylcarbonylamino, where the alkyl, cycloalkyl and         alkoxy radicals mentioned may be partially or fully halogenated         and/or may carry one, two or three of the following radicals:         cyano, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkylaminocarbonyl,         di(C₁-C₄-alkyl)-aminocarbonyl or C₃-C₆-cycloalkyl;     -    is phenyl, phenyl-C₁-C₄-alkyl, phenylcarbonyl, heterocyclyl,         heterocyclyl-C₁-C₄-alkyl or heterocyclylcarbonyl, where the         phenyl or heterocyclyl radical of the six lastmentioned         substituents may be partially or fully halogenated and/or may         carry one to three of the following radicals: nitro, cyano,         C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy;     -   R¹⁹ is hydrogen, C₁-C₆-alkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl;     -   and their agriculturally useful salts.         Furthermore we have found herbicidal compositions which comprise         the cyclohexenone derivatives of the formula I and have very         good herbicidal action. Moreover, we have found methods for         controlling undesirable vegetation using the cyclohexenone         derivatives of the formula I.

Depending on the substitution pattern, the compounds of the formula I may contain one or more chiral centers, in which case they are present as enantiomers or diasteromer mixtures. The invention provides both the pure enantiomers or diastereomers and their mixtures.

The compounds of the formula I may also be present in the form of their agriculturally useful salts, the type of salt generally being immaterial. In general, the salts of those cations and the acid addition salts of those acids are suitable whose cations and anions, respectively, do not negatively affect the herbicidal action of the compounds I.

Suitable cations are, in particular, ions of the alkali metals, preferably lithium, sodium and potassium, of the alkaline earth metals, preferably calcium and magnesium, and of the transition metals, preferably manganese, copper, zinc and iron, and also ammonium, where, if desired, one to four hydrogen atoms may be replaced by C₁-C₄-alkyl, hydroxy-C₁-C₄-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl, hydroxy-C₁-C₄-alkoxy-C₁-C₄-alkyl, phenyl or benzyl, preferably ammonium, dimethylammonium, diisopropylammonium, tetramethylammonium, tetrabutylammonium, 2-(2-hydroxyeth-1-oxy)-eth-1-ylammonium, di(2-hydroxyeth-1-yl)ammonium, trimethylbenzylammonium, furthermore phosphonium ions, sulfonium ions, preferably tri(C₁-C₄-alkyl)sulfonium, and sulfoxonium ions, preferably tri(C₁-C₄-alkyl)sulfoxonium.

Anions of useful acid addition salts are primarily chloride, bromide, fluoride, hydrogen sulfate, sulfate, dihydrogen phosphate, hydrogen phosphate, nitrate, bicarbonate, carbonate, hexafluorosilicate, hexafluorophosphate, benzoate and the anions of C₁-C₄-alkanoic acids, preferably formate, acetate, propionate and butyrate.

For R⁷=hydroxyl or mercapto {Y=O,S}, IIa also represents the tautomeric forms IIa′, IIa″ and IIa′″.

and IIb also represents the tautomeric forms IIb′, IIb″ and IIb′″.

The organic molecular moieties mentioned for the substituents R¹ to R¹⁹ or as radicals on phenyl and heterocyclyl radicals are collective terms for individual enumerations of the particular group members. All hydrocarbon chains, i.e. all alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, haloalkylthio, alkylsulfinyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, N-alkylamino, N,N-dialkylamino, N-haloalkylamino, N-alkoxyamino, N-alkoxy-N-alkylamino, N-alkylcarbonylamino, alkylcarbonyl, haloalkylcarbonyl, alkoxycarbonyl, haloalkoxycarbonyl, alkylthiocarbonyl, alkylcarbonyloxy, alkylaminocarbonyl, dialkylaminocarbonyl, dialkylaminothiocarbonyl, alkoxyalkyl, hydroxyalkoxyalkyl, alkoxyiminoalkyl, phenylalkylcarbonyl, heterocyclylalkylcarbonyl, phenylalkenylcarbonyl, heterocyclylalkenylcarbonyl, N-alkoxy-N-alkylaminocarbonyl, N-alkyl-N-phenylaminocarbonyl, N-alkyl-N-heterocyclylaminocarbonyl, phenylalkyl, heterocyclylalkyl, phenylcarbonylalkyl, heterocyclylcarbonylalkyl, alkoxyalkoxycarbonyl, alkenylcarbonyl, alkenyloxycarbonyl, alkenylaminocarbonyl, N-alkenyl-N-alkylaminocarbonyl, N-alkenyl-N-alkoxyaminocarbonyl, alkynylcarbonyl, alkynyloxycarbonyl, alkynylaminocarbonyl, N-alkynyl-N-alkylaminocarbonyl, N-alkynyl-N-alkoxyaminocarbonyl, alkenyl, alkynyl, haloalkenyl, haloalkynyl, alkenyloxy, alkynyloxy, alkanediyl, alkenediyl, alkadienediyl or alkynediyl moieties can be straight-chain or branched. Unless indicated otherwise, halogenated substituents preferably carry one to five identical or different halogen atoms. The expression halogen represents in each case fluorine, chlorine, bromine or iodine.

Examples of other meanings are:

-   C₁-C₄-alkyl: for example methyl, ethyl, propyl, 1-methylethyl,     butyl, 1-methylpropyl, 2-methylpropyl or 1,1-dimethylethyl; -   C₁-C₄-haloalkyl: a C₁-C₄-alkyl radical as mentioned above which is     partially or fully substituted by fluorine, chlorine, bromine and/or     iodine, i.e., for example, chloromethyl, dichloromethyl,     trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl,     chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl,     2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 2-iodoethyl,     2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl,     2-chloro-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl,     2,2,2-trichloroethyl, pentafluoroethyl, 2-fluoropropyl,     3-fluoropropyl, 2,2-difluoropropyl, 2,3-difluoropropyl,     2-chloropropyl, 3-chloropropyl, 2,3-dichloropropyl, 2-bromopropyl,     3-bromopropyl, 3,3,3-trifluoropropyl, 3,3,3-trichloropropyl,     2,2,3,3,3-pentafluoropropyl, heptafluoropropyl,     1-(fluoromethyl)-2-fluoroethyl, 1-(chloromethyl)-2-chloroethyl,     1-(bromomethyl)-2-bromoethyl, 4-fluorobutyl, 4-chlorobutyl,     4-bromobutyl or nonafluorobutyl; -   C₁-C₆-alkyl, and the alkyl moieties of C₁-C₆-alkylamino,     di(C₁-C₆-alkyl)amino,     N-(C₁-C₆-alkoxy)-N-(C₁-C₆-alkyl)-aminocarbonyl,     N-(C₃-C₆-alkenyl)-N-(C₁-C₆-alkyl)aminocarbonyl,     (C₃-C₆-alkynyl)-N-(C₁-C₆-alkyl)aminocarbonyl,     N-(C₁-C₆-alkyl)-N-phenylaminocarbonyl, and also     N-(C₁-C₆-alkyl)-N-heterocyclylamino-carbonyl: C₁-C₄-alkyl as     mentioned above, and also, for example, n-pentyl, 1-methylbutyl,     2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl,     hexyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 1-methylpentyl,     2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl,     1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl,     2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl,     1,1,2-trimethylpropyl, 1-ethyl-1-methylpropyl or     1-ethyl-3-methylpropyl; -   C₁-C₆-haloalkyl, and the haloalkyl moieties of     N-C₁-C₆-haloalkylamino: C₁-C₄-haloalkyl, as mentioned above, and     also, for example, 5-fluoropentyl, 5-chloropentyl, 5-bromopentyl,     5-iodopentyl, undecafluoropentyl, 6-fluorohexyl, 6-chlorohexyl,     6-bromohexyl, 6-iodohexyl or dodecafluorohexyl; -   C₁-C₄-alkoxy and the alkoxy moieties of     hydroxy-C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkoxycarbonyl:     for example methoxy, ethoxy, propoxy, 1-methylethoxy, butoxy,     1-methylpropoxy, 2-methylpropoxy or 1,1-dimethylethoxy; -   C₁-C₆-alkoxy, and the alkoxy moieties of C₁-C₆-alkoxy-C₃-C₆-alkenyl,     C₁-C₆-alkoxy-C₃-C₆-alkynyl, C₁-C₆-alkoxy-C₂-C₆-alkenyl,     C₁-C₆-alkoxy-C₂-C₆-alkynyl, N-C₁-C₆-alkoxyamino,     N-(C₁-C₆-alkoxy)-N-(C₁-C₆-alkyl)amino,     C₁-C₆-alkoxyimino-C₁-C₆-alkyl,     (C₁-C₆-alkoxy)(C₁-C₆-alkylthio)methyl,     N-(C₁-C₆-alkoxy)-N-(C₁-C₆-alkyl)aminocarbonyl,     N-(C₃-C₆-alkenyl)-N-(C₁-C₆-alkoxy)aminocarbonyl and     N-(C₃-C₆-alkynyl)-N-(C₁-C₆-alkoxy)aminocarbonyl: C₁-C₄-alkoxy as     mentioned above, and also, for example, pentoxy, 1-methylbutoxy,     2-methylbutoxy, 3-methylbutoxy, 1,1-dimethylpropoxy,     1,2-dimethylpropoxy, 2,2-dimethylpropoxy, 1-ethylpropoxy, hexoxy,     1-methylpentoxy, 2-methylpentoxy, 3-methylpentoxy, 4-methylpentoxy,     1,1-dimethylbutoxy, 1,2-dimethylbutoxy, 1,3-dimethylbutoxy,     2,2-dimethylbutoxy, 2,3-dimethylbutoxy, 3,3-dimethylbutoxy,     1-ethylbutoxy, 2-ethylbutoxy, 1,1,2-trimethylpropoxy,     1,2,2-trimethylpropoxy, 1-ethyl-1-methylpropoxy or     1-ethyl-2-methylpropoxy; -   C₁-C₄-haloalkoxy and the haloalkoxy moieties of     C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₁-C₄-haloalkoxy-C₁-C₄-alkoxy,     C₁-C₄-haloalkoxy-C₁-C₆-alkyl, C₁-C₄-haloalkoxy-C₁-C₆-alkoxy,     C₁-C₄-haloalkoxy-C₃-C₆-alkenyl, C₁-C₄-haloalkoxy-C₃-C₆-alkynyl: a     C₁-C₄-alkoxy radical as mentioned above which is partially or fully     substituted by fluorine, chlorine, bromine and/or iodine, i.e., for     example, fluoromethoxy, difluoromethoxy, trifluoromethoxy,     chlorodifluoromethoxy, bromodifluoromethoxy, 2-fluoroethoxy,     2-chloroethoxy, 2-bromomethoxy, 2-iodoethoxy, 2,2-difluoroethoxy,     2,2,2-trifluoroethoxy, 2-chloro-2-fluoroethoxy,     2-chloro-2,2-difluoroethoxy, 2,2-dichloro-2-fluoroethoxy,     2,2,2-trichloroethoxy, pentafluoroethoxy, 2-fluoropropoxy,     3-fluoropropoxy, 2-chloropropoxy, 3-chloropropoxy, 2-bromopropoxy,     3-bromopropoxy, 2,2-difluoropropoxy, 2,3-difluoropropoxy,     2,3-dichloropropoxy, 3,3,3-trifluoropropoxy, 3,3,3-trichloropropoxy,     2,2,3,3,3-pentafluoropropoxy, heptafluoropropoxy,     1-(fluoromethyl)-2-fluoroethoxy, 1-(chloromethyl)-2-chloroethoxy,     1-(bromomethyl)-2-bromoethoxy, 4-fluorobutoxy, 4-chlorobutoxy,     4-bromobutoxy or nonafluorobutoxy; -   C₁-C₆-haloalkoxy: C₁-C₄-haloalkoxy as mentioned above, and also, for     example, 5-fluoropentoxy, 5-chloropentoxy, 5-bromopentoxy,     5-iodopentoxy, undecafluoropentoxy, 6-fluorohexoxy, 6-chlorohexoxy,     6-bromohexoxy, 6-iodohexoxy or dodecafluorohexoxy; -   C₁-C₄-alkylthio (C₁-C₄-alkylsulfanyl: C₁-C₄-alkyl-S—) and the     alkylthio moieties of C₁-C₄-alkylthio-C₁-C₄-alkyl: for example     methylthio, ethylthio, propylthio, 1-methylethylthio, butylthio,     1-methylpropylthio, 2-methylpropylthio or 1,1-dimethylethylthio; -   C₁-C₆-alkylthio, and the alkylthio moieties of     di-(C₁-C₆-alkylthio)methyl, C₁-C₆-alkylthiocarbonyl: C₁-C₄-alkylthio     as mentioned above, and also, for example, pentylthio,     1-methylbutylthio, 2-methylbutylthio, 3-methylbutylthio,     2,2-dimethylpropylthio, 1-ethylpropylthio, hexylthio,     1,1-dimethylpropylthio, 1,2-dimethylpropylthio, 1-methylpentylthio,     2-methylpentylthio, 3-methylpentylthio, 4-methylpentylthio,     1,1-dimethylbutylthio, 1,2-dimethylbutylthio, 1,3-dimethylbutylthio,     2,2-dimethylbutylthio, 2,3-dimethylbutylthio, 3,3-dimethylbutylthio,     1-ethylbutylthio, 2-ethylbutylthio, 1,1,2-trimethylpropylthio,     1,2,2-trimethylpropylthio, 1-ethyl-1-methylpropylthio or     1-ethyl-2-methylpropylthio; -   C₁-C₄-haloalkylthio and the haloalkylthio moieties of     C₁-C₄-haloalkylthio-C₁-C₄-alkyl: a C₁-C₄-alkylthio radical as     mentioned above which is partially or fully substituted by fluorine,     chlorine, bromine and/or iodine, i.e., for example,     fluoromethylthio, difluoromethylthio, trifluoromethylthio,     chlorodifluoromethylthio, bromodifluoromethylthio,     2-fluoroethylthio, 2-chloroethylthio, 2-bromoethylthio,     2-iodoethylthio, 2,2-difluoroethylthio, 2,2,2-trifluoroethylthio,     2,2,2-trichloroethylthio, 2-chloro-2-fluoroethylthio,     2-chloro-2,2-difluoroethylthio, 2,2-dichloro-2-fluoroethylthio,     pentafluoroethylthio, 2-fluoropropylthio, 3-fluoropropylthio,     2-chloropropylthio, 3-chloropropylthio, 2-bromopropylthio,     3-bromopropylthio, 2,2-difluoropropylthio, 2,3-difluoropropylthio,     2,3-dichloropropylthio, 3,3,3-trifluoropropylthio,     3,3,3-trichloropropylthio, 2,2,3,3,3-pentafluoropropylthio,     heptafluoropropylthio, 1-(fluoromethyl)-2-fluoroethylthio,     1-(chloromethyl)-2-chloroethylthio,     1-(bromomethyl)-2-bromoethylthio, 4-fluorobutylthio,     4-chlorobutylthio, 4-bromobutylthio or nonafluorobutylthio; -   C₁-C₆-haloalkylthio: C₁-C₄-haloalkylthio as mentioned above, and     also 5-fluoropentylthio, 5-chloropentylthio, 5-bromopentylthio,     5-iodopentylthio, undecafluoropentylthio, 6-fluorohexylthio,     6-chlorohexylthio, 6-bromohexylthio, 6-iodohexylthio or     dodecafluorohexylthio; -   C₁-C₄-alkylsulfinyl (C₁-C₄-alkyl-S(═O)—): for example,     methylsulfinyl, ethylsulfinyl, propylsulfinyl,     1-methylethylsulfinyl, butylsulfinyl, 1-methylpropylsulfinyl,     2-methylpropylsulfinyl or 1,1-dimethylethylsulfinyl; -   C₁-C₆-alkylsulfinyl: C₁-C₄-alkylsulfinyl as mentioned above, and     also pentylsulfinyl, 1-methylbutylsulfinyl, 2-methylbutylsulfinyl,     3-methylbutylsulfinyl, 2,2-dimethylpropylsulfinyl,     1-ethylpropylsulfinyl, 1,1-dimethylpropylsulfinyl,     1,2-dimethylpropylsulfinyl, hexylsulfinyl, 1-methylpentylsulfinyl,     2-methylpentylsulfinyl, 3-methylpentylsulfinyl,     4-methylpentylsulfinyl, 1,1-dimethylbutylsulfinyl,     1,2-dimethylbutylsulfinyl, 1,3-dimethylbutylsulfinyl,     2,2-dimethylbutylsulfinyl, 2,3-dimethylbutylsulfinyl,     3,3-dimethylbutylsulfinyl, 1-ethylbutylsulfinyl,     2-ethylbutylsulfinyl, 1,1,2-trimethylpropylsulfinyl,     1,2,2-trimethylpropylsulfinyl, 1-ethyl-1-methylpropylsulfinyl or     1-ethyl-2-methylpropylsulfinyl; -   C₁-C₄-haloalkylsulfinyl: a C₁-C₄-alkylsulfinyl radical as mentioned     above which is partially or fully substituted by fluorine, chlorine,     bromine and/or iodine, i.e., for example, fluoromethylsulfinyl,     difluoromethylsulfinyl, trifluoromethylsulfinyl,     chlorodifluoromethylsulfinyl, bromodifluoromethylsulfinyl,     2-fluoroethylsulfinyl, 2-chloroethylsulfinyl, 2-bromoethylsulfinyl,     2-iodoethylsulfinyl, 2,2-difluoroethylsulfinyl,     2,2,2-trifluoroethylsulfinyl, 2,2,2-trichloroethylsulfinyl,     2-chloro-2-fluoroethylsulfinyl, 2-chloro-2,2-difluoroethylsulfinyl,     2,2-dichloro-2-fluoroethylsulfinyl, pentafluoroethylsulfinyl,     2-fluoropropylsulfinyl, 3-fluoropropylsulfinyl,     2-chloropropylsulfinyl, 3-chloropropylsulfinyl,     2-bromopropylsulfinyl, 3-bromopropylsulfinyl,     2,2-difluoropropylsulfinyl, 2,3-difluoropropylsulfinyl,     2,3-dichloropropylsulfinyl, 3,3,3-trifluoropropylsulfinyl,     3,3,3-trichloropropylsulfinyl, 2,2,3,3,3-pentafluoropropylsulfinyl,     heptafluoropropylsulfinyl, 1-(fluoromethyl)-2-fluoroethylsulfinyl,     1-(chloromethyl)-2-chloroethylsulfinyl,     1-(bromomethyl)-2-bromoethylsulfinyl, 4-fluorobutylsulfinyl,     4-chlorobutylsulfinyl, 4-bromobutylsulfinyl or     nonafluorobutylsulfinyl; -   C₁-C₆-haloalkylsulfinyl: C₁-C₄-haloalkylsulfinyl as mentioned above,     and also 5-fluoropentylsulfinyl, 5-chloropentylsulfinyl,     5-bromopentylsulfinyl, 5-iodopentylsulfinyl,     undecafluoropentylsulfinyl, 6-fluorohexylsulfinyl,     6-chlorohexylsulfinyl, 6-bromohexylsulfinyl, 6-iodohexylsulfinyl or     dodecafluorohexylsulfinyl; -   C₁-C₄-alkylsulfonyl (C₁-C₄-alkyl-S(═O)₂—) and the alkylsulfonyl     moieties of C₁-C₄-alkylsulfonyl-C₁-C₄-alkyl: for example     methylsulfonyl, ethylsulfonyl, propylsulfonyl,     1-methylethylsulfonyl, butylsulfonyl, 1-methylpropylsulfonyl,     2-methylpropylsulfonyl or 1,1-dimethylethylsulfonyl; -   C₁-C₆-alkylsulfonyl: C₁-C₄-alkylsulfonyl, as mentioned above, and     also pentylsulfonyl, 1-methylbutylsulfonyl, 2-methylbutylsulfonyl,     3-methylbutylsulfonyl, 1,1-dimethylpropylsulfonyl,     1,2-dimethylpropylsulfonyl, 2,2-dimethylpropylsulfonyl,     1-ethylpropylsulfonyl, hexylsulfonyl, 1-methylpentylsulfonyl,     2-methylpentylsulfonyl, 3-methylpentylsulfonyl,     4-methylpentylsulfonyl, 1,1-dimethylbutylsulfonyl,     1,2-dimethylbutylsulfonyl, 1,3-dimethylbutylsulfonyl,     2,2-dimethylbutylsulfonyl, 2,3-dimethylbutylsulfonyl,     3,3-dimethylbutylsulfonyl, 1-ethylbutylsulfonyl,     2-ethylbutylsulfonyl, 1,1,2-trimethylpropylsulfonyl,     1,2,2-trimethylpropylsulfonyl, 1-ethyl-₁-methylpropylsulfonyl or     1-ethyl-2-methylpropylsulfonyl; -   C₁-C₄-haloalkylsulfonyl: a C₁-C₄-alkylsulfonyl radical as mentioned     above which is partially or fully substituted by fluorine, chlorine,     bromine and/or iodine, and also the haloalkylsulfonyl of     C₁-C₄-haloalkylsulfonyl-C₁-C₄-alkyl: for example,     fluoromethylsulfonyl, difluoromethylsulfonyl,     trifluoromethylsulfonyl, chlorodifluoromethylsulfonyl,     bromodifluoromethylsulfonyl, 2-fluoroethylsulfonyl,     2-chloroethylsulfonyl, 2-bromoethylsulfonyl, 2-iodoethylsulfonyl,     2,2-difluoroethylsulfonyl, 2,2,2-trifluoroethylsulfonyl,     2-chloro-2-fluoroethylsulfonyl, 2-chloro-2,2-difluoroethylsulfonyl,     2,2-dichloro-2-fluoroethylsulfonyl, 2,2,2-trichloroethylsulfonyl,     pentafluoroethylsulfonyl, 2-fluoropropylsulfonyl,     3-fluoropropylsulfonyl, 2-chloropropylsulfonyl,     3-chloropropylsulfonyl, 2-bromopropylsulfonyl,     3-bromopropylsulfonyl, 2,2-difluoropropylsulfonyl,     2,3-difluoropropylsulfonyl, 2,3-dichloropropylsulfonyl,     3,3,3-trifluoropropylsulfonyl, 3,3,3-trichloropropylsulfonyl,     2,2,3,3,3-pentafluoropropylsulfonyl, heptafluoropropylsulfonyl,     1-(fluoromethyl)-2-fluoroethylsulfonyl,     1-(chloromethyl)-2-chloroethylsulfonyl,     1-(bromomethyl)-2-bromoethylsulfonyl, 4-fluorobutylsulfonyl,     4-chlorobutylsulfonyl, 4-bromobutylsulfonyl or     nonafluorobutylsulfonyl; -   C₁-C₆-haloalkylsulfonyl and the haloalkylsulfonyl moieties of     C₁-C₆-haloalkylsulfonyl-C₁-C₆-alkyl: C₁-C₄-haloalkylsulfonyl as     mentioned above, and also 5-fluoropentylsulfonyl,     5-chloropentylsulfonyl, 5-bromopentylsulfonyl, 5-iodopentylsulfonyl,     6-fluorohexylsulfonyl, 6-bromohexylsulfonyl, 6-iodohexylsulfonyl or     dodecafluorohexylsulfonyl; -   C₁-C₆-alkylamino: methylamino, ethylamino, propylamino,     1-methylethylamino, butylamino, 1-methylpropylamino,     2-methylpropylamino, 1,1-dimethylethylamino, pentylamino,     1-methylbutylamino, 2-methylbutylamino, 3-methylbutylamino,     2,2-dimethylpropylamino, 1-ethylpropylamino, hexylamino,     1,1-dimethylpropylamino, 1,2-dimethylpropylamino,     1-methylpentylamino, 2-methylpentylamino, 3-methylpentylamino,     4-methylpentylamino, 1,1-dimethylbutylamino, 1,2-dimethylbutylamino,     1,3-dimethylbutylamino, 2,2-dimethylbutylamino,     2,3-dimethylbutylamino, 3,3-dimethylbutylamino, 1-ethylbutylamino,     2-ethylbutylamino, 1,1,2-trimethylpropylamino,     1,2,2-trimethylpropylamino, 1-ethyl-1-methylpropylamino or     1-ethyl-2-methylpropylamino; -   di(C₁-C₄-alkyl)amino: for example N,N-dimethylamino,     N,N-diethylamino, N,N-dipropylamino, N,N-di(1-methylethyl)-amino,     N,N-dibutylamino, N,N-di(1-methylpropyl)amino,     N,N-di(2-methylpropyl)amino, N,N-di(1,1-dimethylethyl)amino,     N-ethyl-N-methylamino, N-methyl-N-propylamino,     N-methyl-N-(1-methylethyl)amino, N-butyl-N-methylamino,     N-methyl-N-(1-methylpropyl)amino, N-methyl-N-(2-methylpropyl)amino,     N-(1,1-dimethylethyl)-N-methylamino, N-ethyl-N-propylamino,     N-ethyl-N-(1-methylethyl)amino, N-butyl-N-ethylamino,     N-ethyl-N-(1-methylpropyl)amino, N-ethyl-N-(2-methylpropyl)amino,     N-ethyl-N-(1,1-dimethylethyl)amino, N-(1-methylethyl)-N-propylamino,     N-butyl-N-propylamino, N-(1-methylpropyl)-N-propylamino,     N-(2-methylpropyl)-N-propylamino,     N-(1,1-dimethylethyl)-N-propylamino, N-butyl-N-(1-methylethyl)amino,     N-(1-methylethyl)-N-(1-methylpropyl)amino,     N-(-methylethyl)-N-(2-methylpropyl)amino,     N-(1,1-dimethylethyl)-N-(1-methylethyl)amino,     N-butyl-N-(1-methylpropyl)amino, N-butyl-N-(2-methylpropyl)amino,     N-butyl-N-(1,1-dimethylethyl)amino,     N-(1-methylpropyl)-N-(2-methylpropyl)amino,     N-(1,1-dimethylethyl)-N-(1-methylpropyl)amino or     N-(1,1-dimethylethyl)-N-(2-methylpropyl)amino; -   di(C₁-C₆-alkyl)amino: di(C₁-C₄-alkyl)amino as mentioned above, and     also N,N-dipentylamino, N,N-dihexylamino, N-methyl-N-pentylamino,     N-ethyl-N-pentylamino, N-methyl-N-hexylamino or     N-ethyl-N-hexylamino; -   C₁-C₄-alkylcarbonyl: for example methylcarbonyl, ethylcarbonyl,     propylcarbonyl, 1-methylethylcarbonyl, butylcarbonyl,     1-methylpropylcarbonyl, 2-methylpropylcarbonyl or     1,1-dimethylethylcarbonyl; -   C₁-C₆-alkylcarbonyl, and the alkylcarbonyl radicals of     C₁-C₆-alkylcarbonylamino: C₁-C₄-alkylcarbonyl as mentioned above,     and also, for example, pentylcarbonyl, 1-methylbutylcarbonyl,     2-methylbutylcarbonyl, 3-methylbutylcarbonyl,     2,2-dimethylpropylcarbonyl, 1-ethylpropylcarbonyl, hexylcarbonyl,     1,1-dimethylpropylcarbonyl, 1,2-dimethylpropylcarbonyl,     1-methylpentylcarbonyl, 2-methylpentylcarbonyl,     3-methylpentylcarbonyl, 4-methylpentylcarbonyl,     1,1-dimethylbutylcarbonyl, 1,2-dimethylbutylcarbonyl,     1,3-dimethylbutylcarbonyl, 2,2-dimethylbutylcarbonyl,     2,3-dimethylbutylcarbonyl, 3,3-dimethylbutylcarbonyl,     1-ethylbutylcarbonyl, 2-ethylbutylcarbonyl,     1,1,2-trimethylpropylcarbonyl, 1,2,2-trimethylpropylcarbonyl,     1-ethyl-1-methylpropylcarbonyl or 1-ethyl-2-methylpropylcarbonyl; -   C₁-C₄-haloalkylcarbonyl: a C₁-C₄-alkylcarbonyl radical as mentioned     above which is partially or fully substituted by fluorine, chlorine,     bromine and/or iodine, i.e. for example, chloroacetyl,     dichloroacetyl, trichloroacetyl, fluoroacetyl, difluoroacetyl,     trifluoroacetyl, chlorofluoroacetyl, dichlorofluoroacetyl,     chlorodifluoroacetyl, 2-fluoroethylcarbonyl, 2-chloroethylcarbonyl,     2-bromoethylcarbonyl, 2-iodoethylcarbonyl,     2,2-difluoroethylcarbonyl, 2,2,2-trifluoroethylcarbonyl,     2-chloro-2-fluoroethylcarbonyl, 2-chloro-2,2-difluoroethylcarbonyl,     2,2-dichloro-2-fluoroethylcarbonyl, 2,2,2-trichloroethylcarbonyl,     pentafluoroethylcarbonyl, 2-fluoropropylcarbonyl,     3-fluoropropylcarbonyl, 2,2-difluoropropylcarbonyl,     2,3-difluoropropylcarbonyl, 2-chloropropylcarbonyl,     3-chloropropylcarbonyl, 2,3-dichloropropylcarbonyl,     2-bromopropylcarbonyl, 3-bromopropylcarbonyl,     3,3,3-trifluoropropylcarbonyl, 3,3,3-trichloropropylcarbonyl,     2,2,3,3,3-pentafluoropropylcarbonyl, heptafluoropropylcarbonyl,     1-(fluoromethyl)-2-fluoroethylcarbonyl,     1-(chloromethyl)-2-chloroethylcarbonyl,     1-(bromomethyl)-2-bromoethylcarbonyl, 4-fluorobutylcarbonyl,     4-chlorobutylcarbonyl, 4-bromobutylcarbonyl or     nonafluorobutylcarbonyl; -   C₁-C₆-haloalkylcarbonyl: a C₁-C₄-haloalkylcarbonyl radical as     mentioned above, and also 5-fluoropentylcarbonyl,     5-chloropentylcarbonyl, 5-bromopentylcarbonyl,     perfluoropentylcarbonyl, 6-fluorohexylcarbonyl,     6-chlorohexylcarbonyl, 6-bromohexylcarbonyl or     perfluorohexylcarbonyl; -   C₁-C₄-alkoxycarbonyl: for example methoxycarbonyl, ethoxycarbonyl,     propoxycarbonyl, 1-methylethoxycarbonyl, butoxycarbonyl,     1-methylpropoxycarbonyl, 2-methylpropoxycarbonyl or     1,1-dimethylethoxycarbonyl; -   C₁-C₆-alkoxycarbonyl and also the alkoxycarbonyl moieties of     C₁-C₆-alkoxycarbonyl-C₁-C₆-alkyl: C₁-C₄-alkoxycarbonyl as mentioned     above, and also, for example, pentoxycarbonyl,     1-methylbutoxycarbonyl, 2-methylbutoxycarbonyl,     3-methylbutoxycarbonyl, 2,2-dimethylpropoxycarbonyl,     1-ethylpropoxycarbonyl, hexoxycarbonyl, 1,1-dimethylpropoxycarbonyl,     1,2-dimethylpropoxycarbonyl, 1-methylpentoxycarbonyl,     2-methylpentoxycarbonyl, 3-methylpentoxycarbonyl,     4-methylpentoxycarbonyl, 1,1-dimethylbutoxycarbonyl,     1,2-dimethylbutoxycarbonyl, 1,3-dimethylbutoxycarbonyl,     2,2-dimethylbutoxycarbonyl, 2,3-dimethylbutoxycarbonyl,     3,3-dimethylbutoxycarbonyl, 1-ethylbutoxycarbonyl,     2-ethylbutoxycarbonyl, 1,1,2-trimethylpropoxycarbonyl,     1,2,2-trimethylpropoxycarbonyl, 1-ethyl-1-methylpropoxycarbonyl or     1-ethyl-2-methylpropoxycarbonyl; -   C₁-C₄-haloalkoxycarbonyl: a C₁-C₄-alkoxycarbonyl radical as     mentioned above which is partially or fully substituted by fluorine,     chlorine, bromine and/or iodine, i.e., for example     fluoromethoxycarbonyl, difluoromethoxycarbonyl,     trifluoromethoxycarbonyl, chlorodifluoromethoxycarbonyl,     bromodifluoromethoxycarbonyl, 2-fluoroethoxycarbonyl,     2-chloroethoxycarbonyl, 2-bromoethoxycarbonyl, 2-iodoethoxycarbonyl,     2,2-difluoroethoxycarbonyl, 2,2,2-trifluoroethoxycarbonyl,     2-chloro-2-fluoroethoxycarbonyl,     2-chloro-2,2-difluoroethoxycarbonyl,     2,2-dichloro-2-fluoroethoxycarbonyl, 2,2,2-trichloroethoxycarbonyl,     pentafluoroethoxycarbonyl, 2-fluoropropoxycarbonyl,     3-fluoropropoxycarbonyl, 2-chloropropoxycarbonyl,     3-chloropropoxycarbonyl, 2-bromopropoxycarbonyl,     3-bromopropoxycarbonyl, 2,2-difluoropropoxycarbonyl,     2,3-difluoropropoxycarbonyl, 2,3-dichloropropoxycarbonyl,     3,3,3-trifluoropropoxycarbonyl, 3,3,3-trichloropropoxycarbonyl,     2,2,3,3,3-pentafluoropropoxycarbonyl, heptafluoropropoxycarbonyl,     1-(fluoromethyl)-2-fluoroethoxycarbonyl,     1-(chloromethyl)-2-chloroethoxycarbonyl,     1-(bromomethyl)-2-bromoethoxycarbonyl, 4-fluorobutoxycarbonyl,     4-chlorobutoxycarbonyl, 4-bromobutoxycarbonyl or     4-iodobutoxycarbonyl; -   C₁-C₆-haloalkoxycarbonyl: a C₁-C₄-haloalkoxycarbonyl radical as     mentioned above, and also 5-fluoropentoxycarbonyl,     5-chloropentoxycarbonyl, 5-bromopentoxycarbonyl,     6-fluorohexoxycarbonyl, 6-chlorohexoxycarbonyl or     6-bromohexoxycarbonyl; -   (C₁-C₄-alkyl)carbonyloxy: acetyloxy, ethylcarbonyloxy,     propylcarbonyloxy, 1-methylethylcarbonyloxy, butylcarbonyloxy,     1-methylpropylcarbonyloxy, 2-methylpropylcarbonyloxy or     1,1-dimethylethylcarbonyloxy; -   (C₁-C₄-alkylamino)carbonyl: for example methylaminocarbonyl,     ethylaminocarbonyl, propylaminocarbonyl, 1-methylethylaminocarbonyl,     butylaminocarbonyl, 1-methylpropylaminocarbonyl,     2-methylpropylaminocarbonyl or 1,1-dimethylethylaminocarbonyl; -   (C₁-C₆-alkylamino)carbonyl: (C₁-C₄-alkylamino)carbonyl as mentioned     above, and also, for example, pentylaminocarbonyl,     1-methylbutylaminocarbonyl, 2-methylbutylaminocarbonyl,     3-methylbutylaminocarbonyl, 2,2-dimethylpropylaminocarbonyl,     1-ethylpropylaminocarbonyl, hexylaminocarbonyl,     1,1-dimethylpropylaminocarbonyl, 1,2-dimethylpropylaminocarbonyl,     1-methylpentylaminocarbonyl, 2-methylpentylaminocarbonyl,     3-methylpentylaminocarbonyl, 4-methylpentylaminocarbonyl,     1,1-dimethylbutylaminocarbonyl, 1,2-dimethylbutylaminocarbonyl,     1,3-dimethylbutylaminocarbonyl, 2,2-dimethylbutylaminocarbonyl,     2,3-dimethylbutylaminocarbonyl, 3,3-dimethylbutylaminocarbonyl,     1-ethylbutylaminocarbonyl, 2-ethylbutylaminocarbonyl,     1,1,2-trimethylpropylaminocarbonyl,     1,2,2-trimethylpropylaminocarbonyl,     1-ethyl-1-methylpropylaminocarbonyl or     1-ethyl-2-methylpropylaminocarbonyl; -   di(C₁-C₄-alkyl)aminocarbonyl: for example N,N-dimethylaminocarbonyl,     N,N-diethylaminocarbonyl, N,N-di(1-methylethyl)aminocarbonyl,     N,N-dipropylaminocarbonyl, N,N-dibutylaminocarbonyl,     N,N-di(1-methylpropyl)-aminocarbonyl,     N,N-di(2-methylpropyl)aminocarbonyl,     N,N-di(1,1-dimethylethyl)aminocarbonyl,     N-ethyl-N-methylaminocarbonyl, N-methyl-N-propylaminocarbonyl,     N-methyl-N-(1-methylethyl)aminocarbonyl,     N-butyl-N-methylaminocarbonyl,     N-methyl-N-(1-methylpropyl)aminocarbonyl,     N-methyl-N-(2-methylpropyl)aminocarbonyl,     N-(1,1-dimethylethyl)-N-methylaminocarbonyl,     N-ethyl-N-propylaminocarbonyl,     N-ethyl-N-(1-methylethyl)-aminocarbonyl,     N-butyl-N-ethylaminocarbonyl,     N-ethyl-N-(1-methylpropyl)aminocarbonyl,     N-ethyl-N-(2-methylpropyl)aminocarbonyl,     N-ethyl-N-(1,1-dimethylethyl)aminocarbonyl,     N-(1-methylethyl)-N-propylaminocarbonyl,     N-butyl-N-propylaminocarbonyl,     N-(1-methylpropyl)-N-propylaminocarbonyl,     N-(2-methylpropyl)-N-propylaminocarbonyl,     N-(1,1-dimethylethyl)-N-propylaminocarbonyl,     N-butyl-N-(1-methylethyl)aminocarbonyl,     N-(1-methylethyl)-N-(1-methylpropyl)aminocarbonyl,     N-(1-methylethyl)-N-(2-methylpropyl)aminocarbonyl,     N-(1,1-dimethylethyl)-N-(1-methylethyl)aminocarbonyl,     N-butyl-N-(1-methylpropyl)-aminocarbonyl,     N-butyl-N-(2-methylpropyl)aminocarbonyl,     N-butyl-N-(1,1-dimethylethyl)aminocarbonyl,     N-(1-methylpropyl)-N-(2-methylpropyl)aminocarbonyl,     N-(1,1-dimethylethyl)-N-(1-methylpropyl)aminocarbonyl or     N-(1,1-dimethylethyl)-N-(2-methylpropyl)aminocarbonyl; -   di(C₁-C₆-alkyl)aminocarbonyl: di(C₁-C₄-alkyl)aminocarbonyl as     mentioned above, and also, for example,     N-methyl-N-pentylaminocarbonyl,     N-methyl-N-(1-methylbutyl)aminocarbonyl,     N-methyl-N-(2-methylbutyl)aminocarbonyl,     N-methyl-N-(3-methylbutyl)aminocarbonyl,     N-methyl-N-(2,2-dimethylpropyl)aminocarbonyl,     N-methyl-N-(1-ethylpropyl)-aminocarbonyl,     N-methyl-N-hexylaminocarbonyl,     N-methyl-N-(1,1-dimethylpropyl)aminocarbonyl,     N-methyl-N-(1,2-dimethylpropyl)aminocarbonyl,     N-methyl-N-(1-methylpentyl)aminocarbonyl,     N-methyl-N-(2-methylpentyl)aminocarbonyl,     N-methyl-N-(3-methylpentyl)aminocarbonyl,     N-methyl-N-(4-methylpentyl)aminocarbonyl,     N-methyl-N-(1,1-dimethylbutyl)aminocarbonyl,     N-methyl-N-(1,2-dimethylbutyl)aminocarbonyl,     N-methyl-N-(1,3-dimethylbutyl)aminocarbonyl,     N-methyl-N-(2,2-dimethylbutyl)aminocarbonyl,     N-methyl-N-(2,3-dimethylbutyl)aminocarbonyl,     N-methyl-N-(3,3-dimethylbutyl)aminocarbonyl,     N-methyl-N-(1-ethylbutyl)aminocarbonyl,     N-methyl-N-(2-ethylbutyl)aminocarbonyl,     N-methyl-N-(1,1,2-trimethylpropyl)aminocarbonyl,     N-methyl-N-(1,2,2-trimethylpropyl)aminocarbonyl,     N-methyl-N-(1-ethyl-1-methylpropyl)aminocarbonyl,     N-methyl-N-(1-ethyl-2-methylpropyl)aminocarbonyl,     N-ethyl-N-pentylaminocarbonyl,     N-ethyl-N-(1-methylbutyl)aminocarbonyl,     N-ethyl-N-(2-methylbutyl)aminocarbonyl,     N-ethyl-N-(3-methylbutyl)aminocarbonyl,     N-ethyl-N-(2,2-dimethylpropyl)aminocarbonyl,     N-ethyl-N-(1-ethylpropyl)aminocarbonyl,     N-ethyl-N-hexylaminocarbonyl,     N-ethyl-N-(1,1-dimethylpropyl)aminocarbonyl,     N-ethyl-N-(1,2-dimethylpropyl)aminocarbonyl,     N-ethyl-N-(1-methylpentyl)aminocarbonyl,     N-ethyl-N-(2-methylpentyl)aminocarbonyl,     N-ethyl-N-(3-methylpentyl)aminocarbonyl,     N-ethyl-N-(4-methylpentyl)aminocarbonyl,     N-ethyl-N-(1,1-dimethylbutyl)aminocarbonyl,     N-ethyl-N-(1,2-dimethylbutyl)aminocarbonyl,     N-ethyl-N-(1,3-dimethylbutyl)aminocarbonyl,     N-ethyl-N-(2,2-dimethylbutyl)aminocarbonyl,     N-ethyl-N-(2,3-dimethylbutyl)aminocarbonyl,     N-ethyl-N-(3,3-dimethylbutyl)aminocarbonyl,     N-ethyl-N-(1-ethylbutyl)aminocarbonyl,     N-ethyl-N-(2-ethylbutyl)aminocarbonyl,     N-ethyl-N-(1,1,2-trimethylpropyl)aminocarbonyl,     N-ethyl-N-(1,2,2-trimethylpropyl)aminocarbonyl,     N-ethyl-N-(1-ethyl-1-methylpropyl)aminocarbonyl,     N-ethyl-N-(1-ethyl-2-methylpropyl)aminocarbonyl,     N-propyl-N-pentylaminocarbonyl, N-butyl-N-pentylaminocarbonyl,     N,N-dipentylaminocarbonyl, N-propyl-N-hexylaminocarbonyl,     N-butyl-N-hexylaminocarbonyl, N-pentyl-N-hexylaminocarbonyl or     N,N-dihexylaminocarbonyl; -   di(C₁-C₆-alkyl)aminothiocarbonyl: for example     N,N-dimethylaminothiocarbonyl, N,N-diethylaminothiocarbonyl,     N,N-di(1-methylethyl)aminothiocarbonyl,     N,N-dipropylaminothiocarbonyl, N,N-dibutylaminothiocarbonyl,     N,N-di(1-methylpropyl)aminothiocarbonyl,     N,N-di(2-methylpropyl)aminothiocarbonyl,     N,N-di(1,1-dimethylethyl)aminothiocarbonyl,     N-ethyl-N-methylaminothiocarbonyl,     N-methyl-N-propylaminothiocarbonyl,     N-methyl-N-(1-methylethyl)aminothiocarbonyl,     N-butyl-N-methylaminothiocarbonyl,     N-methyl-N-(1-methylpropyl)aminothiocarbonyl,     N-methyl-N-(2-methylpropyl)aminothiocarbonyl,     N-(1,1-dimethylethyl)-N-methylaminothiocarbonyl,     N-ethyl-N-propylaminothiocarbonyl,     N-ethyl-N-(1-methylethyl)aminothiocarbonyl,     N-butyl-N-ethylaminothiocarbonyl,     N-ethyl-N-(1-methylpropyl)aminothiocarbonyl,     N-ethyl-N-(2-methylpropyl)aminothiocarbonyl,     N-ethyl-N-(1,1-dimethylethyl)aminothiocarbonyl,     N-(1-methylethyl)-N-propylaminothiocarbonyl,     N-butyl-N-propylaminothiocarbonyl,     N-(1-methylpropyl)-N-propylaminothiocarbonyl,     N-(2-methylpropyl)-N-propylaminothiocarbonyl,     N-(1,1-dimethylethyl)-N-propylaminothiocarbonyl,     N-butyl-N-(1-methylethyl)aminothiocarbonyl,     N-(1-methylethyl)-N-(1-methylpropyl)aminothiocarbonyl,     N-(1-methylethyl)-N-(2-methylpropyl)aminothiocarbonyl,     N-(1,1-dimethylethyl)-N-(1-methylethyl)aminothiocarbonyl,     N-butyl-N-(1-methylpropyl)aminothiocarbonyl,     N-butyl-N-(2-methylpropyl)aminothiocarbonyl,     N-butyl-N-(1,1-dimethylethyl)aminothiocarbonyl,     N-(1-methylpropyl)-N-(2-methylpropyl)aminothiocarbonyl,     N-(1,1-dimethylethyl)-N-(1-methylpropyl)aminothiocarbonyl,     N-(1,1-dimethylethyl)-N-(2-methylpropyl)aminothiocarbonyl,     N-methyl-N-pentylaminothiocarbonyl,     N-methyl-N-(1-methylbutyl)aminothiocarbonyl,     N-methyl-N-(2-methylbutyl)aminothiocarbonyl,     N-methyl-N-(3-methylbutyl)aminothiocarbonyl,     N-methyl-N-(2,2-dimethylpropyl)aminothiocarbonyl,     N-methyl-N-(1-ethylpropyl)aminothiocarbonyl,     N-methyl-N-hexylaminothiocarbonyl,     N-methyl-N-(1,1-dimethylpropyl)aminothiocarbonyl,     N-methyl-N-(1,2-dimethylpropyl)aminothiocarbonyl,     N-methyl-N-(1-methylpentyl)aminothiocarbonyl,     N-methyl-N-(2-methylpentyl)aminothiocarbonyl,     N-methyl-N-(3-methylpentyl)aminothiocarbonyl,     N-methyl-N-(4-methylpentyl)aminothiocarbonyl,     N-methyl-N-(1,1-dimethylbutyl)aminothiocarbonyl,     N-methyl-N-(1,2-dimethylbutyl)aminothiocarbonyl,     N-methyl-N-(1,3-dimethylbutyl)aminothiocarbonyl,     N-methyl-N-(2,2-dimethylbutyl)aminothiocarbonyl,     N-methyl-N-(2,3-dimethylbutyl)aminothiocarbonyl,     N-methyl-N-(3,3-dimethylbutyl)aminothiocarbonyl,     N-methyl-N-(1-ethylbutyl)aminothiocarbonyl,     N-methyl-N-(2-ethylbutyl)aminothiocarbonyl,     N-methyl-N-ethyl-N-(1,1,2-trimethylpropyl)aminothiocarbonyl,     N-methyl-N-(1,2,2-trimethylpropyl)aminothiocarbonyl,     N-methyl-N-(1-ethyl-1-methylpropyl)aminothiocarbonyl,     N-methyl-N-(1-ethyl-2-methylpropyl)aminothiocarbonyl,     N-ethyl-N-pentylaminothiocarbonyl,     N-ethyl-N-(1-methylbutyl)aminothiocarbonyl,     N-ethyl-N-(2-methylbutyl)aminothiocarbonyl,     N-ethyl-N-(3-methylbutyl)aminothiocarbonyl,     N-ethyl-N-(2,2-dimethylpropyl)aminothiocarbonyl,     N-ethyl-N-(1-ethylpropyl)aminothiocarbonyl,     N-ethyl-N-hexylaminothiocarbonyl,     N-ethyl-N-(1,1-dimethylpropyl)aminothiocarbonyl,     N-ethyl-N-(1,2-dimethylpropyl)aminothiocarbonyl,     N-ethyl-N-(1-methylpentyl)aminothiocarbonyl,     N-ethyl-N-(2-methylpentyl)aminothiocarbonyl,     N-ethyl-N-(3-methylpentyl)aminothiocarbonyl,     N-ethyl-N-(4-methylpentyl)aminothiocarbonyl,     N-ethyl-N-(1,1-dimethylbutyl)aminothiocarbonyl,     N-ethyl-N-(1,2-dimethylbutyl)aminothiocarbonyl,     N-ethyl-N-(1,3-dimethylbutyl)aminothiocarbonyl,     N-ethyl-N-(2,2-dimethylbutyl)aminothiocarbonyl,     N-ethyl-N-(2-,3-dimethylbutyl)aminothiocarbonyl,     N-ethyl-N-(3,3-dimethylbutyl)aminothiocarbonyl,     N-ethyl-N-(1-ethylbutyl)aminothiocarbonyl,     N-ethyl-N-(2-ethylbutyl)aminothiocarbonyl,     N-ethyl-N-(1,1,2-trimethylpropyl)aminothiocarbonyl,     N-ethyl-N-(1,2,2-trimethylpropyl)aminothiocarbonyl,     N-ethyl-N-(1-ethyl-1-methylpropyl)aminothiocarbonyl,     N-ethyl-N-(1-ethyl-2-methylpropyl)aminothiocarbonyl,     N-propyl-N-pentylaminothiocarbonyl,     N-butyl-N-pentylaminothiocarbonyl, N,N-dipentylaminothiocarbonyl,     N-propyl-N-hexylaminothiocarbonyl, N-butyl-N-hexylaminothiocarbonyl,     N-pentyl-N-hexylaminothiocarbonyl or N,N-dihexylaminothiocarbonyl; -   C₁-C₆-hydroxyalkyl: C₁-C₆-alkyl which is substituted by one to three     OH groups, for example hydroxymethyl, 1-hydroxyethyl,     2-hydroxyethyl, 1,2-bishydroxyethyl, 1-hydroxypropyl,     2-hydroxypropyl, 3-hydroxypropyl, 4-hydroxybutyl,     2,2-dimethyl-3-hydroxypropyl; -   phenyl-C₁-C₆-alkyl: C₁-C₆-alkyl which is substituted by a phenyl     radical, for example benzyl, 1-phenylethyl and 2-phenylethyl, where     the phenyl radical may, in the manner mentioned, be partially or     fully halogenated or may carry one to three of the substituents     mentioned above for phenyl; correspondingly,     heterocyclyl-C₁-C₆-alkyl is a C₁-C₆-alkyl. which is substituted by a     heterocyclyl radical; -   C₁-C₆-alkoxy-C₁-C₆-alkyl: C₁-C₆-alkyl which is substituted by     C₁-C₆-alkoxy as mentioned above, i.e., for example, methoxymethyl,     ethoxymethyl, propoxymethyl, (1-methylethoxy)methyl, butoxymethyl,     (1-methylpropoxy)methyl, (2-methylpropoxy)methyl,     (1,1-dimethylethoxy)methyl, 2-(methoxy)ethyl, 2-(ethoxy)ethyl,     2-(propoxy)ethyl, 2-(1-methylethoxy)ethyl, 2-(butoxy)ethyl,     2-(1-methylpropoxy)ethyl, 2-(2-methylpropoxy)ethyl,     2-(1,1-dimethylethoxy)ethyl, 2-(methoxy)propyl, 2-(ethoxy)propyl,     2-(propoxy)propyl, 2-(1-methylethoxy)propyl, 2-(butoxy)propyl,     2-(1-methylpropoxy)propyl, 2-(2-methylpropoxy)propyl,     2-(1,1-dimethylethoxy)propyl, 3-(methoxy)propyl, 3-(ethoxy)propyl,     3-(propoxy)propyl, 3-(1-methylethoxy)propyl, 3-(butoxy)propyl,     3-(1-methylpropoxy)propyl, 3-(2-methylpropoxy)propyl,     3-(1,1-dimethylethoxy)propyl, 2-(methoxy)butyl, 2-(ethoxy)butyl,     2-(propoxy)butyl, 2-(1-methylethoxy)butyl, 2-(butoxy)butyl,     2-(1-methylpropoxy)butyl, 2-(2-methylpropoxy)butyl,     2-(1,1-dimethylethoxy)butyl, 3-(methoxy)butyl, 3-(ethoxy)butyl,     3-(propoxy)butyl, 3-(1-methylethoxy)butyl, 3-(butoxy)butyl,     3-(1-methylpropoxy)butyl, 3-(2-methylpropoxy)butyl,     3-(1,1-dimethylethoxy)butyl, 4-(methoxy)butyl, 4-(ethoxy)butyl,     4-(propoxy)butyl, 4-(1-methylethoxy)butyl, 4-(butoxy)butyl,     4-(1-methylpropoxy)butyl, 4-(2-methylpropoxy)butyl or     4-(1,1-dimethylethoxy)butyl; -   C₁-C₆-alkoxy-C₁-C₆-alkoxy, and the alkoxyalkoxy moieties of     C₁-C₆-alkoxy-C₁-C₆-alkoxycarbonyl: C₁-C₆-alkoxy which is substituted     by C₁-C₆-alkoxy as mentioned above, i.e, for example,     methoxymethoxy, ethoxymethoxy, propoxymethoxy,     (1-methylethoxy)methoxy, butoxymethoxy, (1-methylpropoxy)methoxy,     (2-methylpropoxy)methoxy, (1,1-dimethylethoxy)methoxy,     2-(methoxy)ethoxy, 2-(ethoxy)ethoxy, 2-(propoxy)ethoxy,     2-(1-methylethoxy)ethoxy, 2-(butoxy)ethoxy,     2-(1-methylpropoxy)ethoxy, 2-(2-methylpropoxy)ethoxy,     2-(1,1-dimethylethoxy)ethoxy, 2-(methoxy)propoxy, 2-(ethoxy)propoxy,     2-(propoxy)propoxy, 2-(1-methylethoxy)propoxy, 2-(butoxy)propoxy,     2-(1-methylpropoxy)propoxy, 2-(2-methylpropoxy)propoxy,     2-(1,1-dimethylethoxy)propoxy, 3-(methoxy)propoxy,     3-(ethoxy)propoxy, 3-(propoxy)propoxy, 3-(1-methylethoxy)propoxy,     3-(butoxy)propoxy, 3-(1-methylpropoxy)propoxy,     3-(2-methylpropoxy)propoxy, 3-(1,1-dimethylethoxy)propoxy,     2-(methoxy)butoxy, 2-(ethoxy)butoxy, 2-(propoxy)butoxy,     2-(1-methylethoxy)butoxy, 2-(butoxy)butoxy,     2-(1-methylpropoxy)butoxy, 2-(2-methylpropoxy)butoxy,     2-(1,1-dimethylethoxy)butoxy, 3-(methoxy)butoxy, 3-(ethoxy)butoxy,     3-(propoxy)butoxy, 3-(1-methylethoxy)butoxy, 3-(butoxy)butoxy,     3-(1-methylpropoxy)butoxy, 3-(2-methylpropoxy)butoxy,     3-(1,1-dimethylethoxy)butoxy, 4-(methoxy)butoxy, 4-(ethoxy)butoxy,     4-(propoxy)butoxy, 4-(1-methylethoxy)butoxy, 4-(butoxy)butoxy,     4-(1-methylpropoxy)butoxy, 4-(2-methylpropoxy)butoxy or     4-(1,1-dimethylethoxy)butoxy; -   C₃-C₆-alkenyl, and the alkenyl moieties of C₃-C₆-alkenylcarbonyl,     C₃-C₆-alkenyloxy, C₃-C₆-alkenyloxycarbonyl,     C₃-C₆-alkenylaminocarbonyl,     N-(C₃-C₆-alkenyl)-N-(C₁-C₆-alkyl)aminocarbonyl,     N-(C₃-C₆-alkenyl)-N-(C₁-C₆-alkoxy)aminocarbonyl: for example     prop-2-en-1-yl, prop-1-en-3-yl, but-1-en-4-yl,     1-methylprop-2-en-1-yl, 2-methylprop-2-en-1-yl, 2-buten-1-yl,     1-penten-3-yl, 1-penten-4-yl, 2-penten-4-yl, 1-methylbut-2-en-1-yl,     2-methylbut-2-en-1-yl, 3-methylbut-2-en-1-yl, 1-methylbut-3-en-1-yl,     2-methylbut-3-en-1-yl, 3-methyl-but-3-en-1-yl,     1,1-dimethylprop-2-en-1-yl, 1,2-dimethylprop-2-en-1-yl,     1-ethylprop-2-en-1-yl, hex-3-en-1-yl, hex-4-en-1-yl, hex-5-en-1-yl,     1-methylpent-3-en-1-yl, 2-methylpent-3-en-1-yl,     3-methylpent-3-en-1-yl, 4-methylpent-3-en-1-yl,     1-methylpent-4-en-1-yl, 2-methylpent-4-en-1-yl,     3-methylpent-4-en-1-yl, 4-methylpent-4-en-1-yl,     1,1-dimethylbut-2-en-1-yl, 1,1-dimethylbut-3-en-1-yl,     1,2-dimethylbut-2-en-1-yl, 1,2-dimethylbut-3-en-1-yl,     1,3-dimethylbut-2-en-1-yl, 1,3-dimethylbut-3-en-1-yl,     2,2-dimethylbut-3-en-1-yl, 2,3-dimethylbut-2-en-1-yl,     2,3-dimethylbut-3-en-1-yl, 3,3-dimethylbut-2-en-1-yl,     1-ethylbut-2-en-1-yl, 1-ethylbut-3-en-1-yl, 2-ethylbut-2-en-1-yl,     2-ethylbut-3-en-1-yl, 1,1,2-trimethylprop-2-en-1-yl,     1-ethyl-1-methylprop-2-en-1-yl or 1-ethyl-2-methylprop-2-en-1-yl; -   C₂-C₆-alkenyl, and the alkenyl moieties of C₂-C₆-alkenylcarbonyl,     phenyl-C₂-C₆-alkenylcarbonyl and heterocyclyl-C₂-C₆-alkenylcarbonyl:     C₃-C₆-alkenyl as mentioned above, and also ethenyl; -   C₃-C₆-haloalkenyl: a C₃-C₆-alkenyl radical as mentioned above which     is partially or fully substituted by fluorine, chlorine, bromine     and/or iodine, i.e., for example, 2-chloroallyl, 3-chloroallyl,     2,3-dichloroallyl, 3,3-dichloroallyl, 2,3,3-trichloroallyl,     2,3-dichlorobut-2-enyl, 2-bromoallyl, 3-bromoallyl,     2,3-dibromoallyl, 3,3-dibromoallyl, 2,3,3-tribromoallyl or     2,3-dibromobut-2-enyl; -   C₃-C₆-alkynyl, and the alkynyl moieties of C₃-C₆-alkynylcarbonyl,     C₃-C₆-alkynyloxy, C₃-C₆-alkynyloxycarbonyl,     C₃-C₆-alkynylaminocarbonyl,     N-(C₃-C₆-alkynyl)-N-(C₁-C₆-alkyl)aminocarbonyl,     N-(C₃-C₆-alkynyl)-N-(C₁-C₆-alkoxy)aminocarbonyl: for example     propargyl, but-1-yn-3-yl, but-1-yn-4-yl, but-2-yn-1-yl,     pent-1-yn-3-yl, pent-1-yn-4-yl, pent-1-yn-5-yl, pent-2-yn-1-yl,     pent-2-yn-4-yl, pent-2-yn-5-yl, 3-methylbut-1-yn-3-yl,     3-methylbut-1-yn-4-yl, hex-1-yn-3-yl, hex-1-yn-4-yl, hex-1-yn-5-yl,     hex-1-yn-6-yl, hex-2-yn-1-yl, hex-2-yn-4-yl, hex-2-yn-5-yl,     hex-2-yn-6-yl, hex-3-yn-1-yl, hex-3-yn-2-yl, 3-methylpent-1-yn-3-yl,     3-methylpent-1-yn-4-yl, 3-methylpent-1-yn-5-yl,     4-methylpent-2-yn-4-yl or 4-methylpent-2-yn-5-yl; -   C₂-C₆-alkynyl, and the alkynyl moieties of C₂-C₆-alkynylcarbonyl:     C₃-C₆-alkynyl as mentioned above, and also ethynyl; -   C₃-C₆-haloalkynyl: a C₃-C₆-alkynyl radical as mentioned above which     is partially or fully substituted by fluorine, chlorine, bromine     and/or iodine, i.e., for example, 1,1-difluoroprop-2-yn-1-yl,     3-iodoprop-2-yn-1-yl, 4-fluorobut-2-yn-1-yl, 4-chlorobut-2-yn-1-yl,     1,1-difluorobut-2-yn-1-yl, 4-iodobut-3-yn-1-yl,     5-fluoropent-3-yn-1-yl, 5-iodopent-4-yn-1-yl, 6-fluorohex-4-yn-1-yl     or 6-iodohex-5-yn-1-yl; -   C₁-C₆-alkanediyl: methanediyl, ethane-1,1-diyl, ethane-1,2-diyl,     propane-1,1-diyl, propane-1,2-diyl, propane-1,3-diyl,     propane-2,2-diyl, butane-1,1-diyl, butane-1,2-diyl, butane-1,3-diyl,     butane-1,4-diyl, 2-methylpropane-1,3-diyl, 2-methylpropane-1,2-diyl,     2-methylpropane-1,1-diyl, 1-methylpropane-1,2-diyl,     1-methylpropane-2,2-diyl, 1-methylpropane-1,1-diyl,     pentane-1,1-diyl, pentane-1,2-diyl, pentane-1,3-diyl,     pentane-1,5-diyl, pentane-2,3-diyl, pentane-2,2-diyl,     1-methylbutane-1,1-diyl, 1-methylbutane-1,2-diyl,     1-methylbutane-1,3-diyl, 1-methylbutane-1,4-diyl,     2-methylbutane-1,1-diyl, 2-methylbutane-.1,2-diyl,     2-methylbutane-1,3-diyl, 2-methylbutane-1,4-diyl,     2,2-dimethylpropane-1,1-diyl, 2,2-dimethylpropane-1,3-diyl,     1,1-dimethylpropane-1,3-diyl, 1,1-dimethylpropane-1,2-diyl,     2,3-dimethylpropane-1,3-diyl, 2,3-dimethylpropane-1,2-diyl,     1,3-dimethylpropane-1,3-diyl, hexane-1,1-diyl, hexane-1,2-diyl,     hexane-1,3-diyl, hexane-1,4-diyl, hexane-1,5-diyl, hexane-1,6-diyl,     hexane-2,5-diyl, 2-methylpentane-1,1-diyl, 1-methylpentane-1,2-diyl,     1-methylpentane-1,3-diyl, 1-methylpentane-1,4-diyl,     1-methylpentane-1,5-diyl, 2-methylpentane-1,1-diyl,     2-methylpentane-1,2-diyl, 2-methylpentane-1,3-diyl,     2-methylpentane-1,4-diyl, 2-methylpentane-1,5-diyl,     3-methylpentane-1,1-diyl, 3-methylpentane-1,2-diyl,     3-methylpentane-1,3-diyl, 3-methylpentane-1,4-diyl,     3-methylpentane-1,5-diyl, 1,1-dimethylbutane-1,2-diyl,     1,1-dimethylbutane-1,3-diyl, 1,1-dimethylbutane-1,4-diyl,     1,2-dimethylbutane-1,1-diyl, 1,2-dimethylbutane-1,2-diyl,     1,2-dimethylbutane-1,3-diyl, 1,2-dimethylbutane-1,4-diyl,     1,3-dimethylbutane-1,1-diyl, 1,3-dimethylbutane-1,2-diyl,     1,3-dimethylbutane-1,3-diyl, 1,3-dimethylbutane-1,4-diyl,     1-ethylbutane-1,1-diyl, 1-ethylbutane-1,2-diyl,     1-ethylbutane-1,3-diyl, 1-ethylbutane-1,4-diyl,     2-ethylbutane-1,1-diyl, 2-ethylbutane-1,2-diyl,     2-ethylbutane-1,3-diyl, 2-ethylbutane-1,4-diyl,     2-ethylbutane-2,3-diyl, 2,2-dimethylbutane-1,1-diyl,     2,2-dimethylbutane-1,3-diyl, 2,2-dimethylbutane-1,4-diyl,     1-isopropylpropane-1,1-diyl, 1-isopropylpropane-1,2-diyl,     1-isopropylpropane-1,3-diyl, 2-isopropylpropane-1,1-diyl,     2-isopropylpropane-1,2-diyl, 2-isopropylpropane-1,3-diyl,     1,2,3-trimethylpropane-1,1-diyl, 1,2,3-trimethylpropane-1,2-diyl or     1,2,3-trimethylpropane-1,3-diyl; -   C₂-C₆-alkenediyl: ethene-1,1-diyl, ethene-1,2-diyl,     1-propene-1,1-diyl, 1-propene-1,2-diyl, 1-propene-1,3-diyl,     2-propene-1,1-diyl, 2-propene-1,2-diyl, 2-propene-1,3-diyl,     1-butene-1,1-diyl, 1-butene-1,2-diyl, 1-butene-1,3-diyl,     1-butene-1,4-diyl, 2-butene-1,1-diyl, 2-butene-1,2-diyl,     2-butene-1,3-diyl, 2-butene-1,4-diyl, 3-butene-1,1-diyl,     3-butene-1,2-diyl, 3-butene-1,3-diyl, 3-butene-1,4-diyl,     1-methyl-1-propene-1,2-diyl, 1-methyl-1-propene-1,3-diyl,     1-methyl-2-propene-1,1-diyl, 1-methyl-2-propene-1,2-diyl,     1-methyl-2-propene-1,3-diyl, 2-methyl-1,1-propene-1,1-diyl,     2-methyl-1-propene-1,3-diyl, 3-butene-1,1-diyl, 3-butene-1,2-diyl,     3-butene-1,3-diyl, 3-butene-1,4-diyl, 1-pentene-1,1-diyl,     1-pentene-1,2-diyl, 1-pentene-1,3-diyl, 1-pentene-1,4-diyl,     1-pentene-1,5-diyl, 1-hexene-1,1-diyl, 1-hexene-1,2-diyl,     1-hexene-1,3-diyl, 1-hexene-1,4-diyl, 1-hexene-1,5-diyl or     1-hexene-1,6-diyl; -   C₂-C₆-alkadienediyl: 1,3-butadiene-1,1-diyl, 1,3-butadiene-1,2-diyl,     1,3-butadiene-1,3-diyl, 1,3-butadiene-1,4-diyl,     1,3-pentadiene-1,1-diyl, 1,3-pentadiene-1,2-diyl,     1,3-pentadiene-1,3-diyl, 1,3-pentadiene-1,4-diyl,     1,3-pentadiene-1,5-diyl, 2,4-pentadiene-1,1-diyl,     2,4-pentadiene-1,2-diyl, 2,4-pentadiene-1,3-diyl,     2,4-pentadiene-1,4-diyl, 2,4-pentadiene-1,5-diyl,     1-methyl-1,3-butadiene-1,4-diyl, 1,3-hexadiene-1,1-diyl,     1,3-hexadiene-1,2-diyl, 1,3-hexadiene-1,3-diyl,     1,3-hexadiene-1,4-diyl, 1,3-hexadiene-1,5-diyl,     1,3-hexadiene-1,6-diyl, 1-methyl-1,3-pentadiene-1,2-diyl,     1-methyl-1,3-pentadiene-1,3-diyl, 1-methyl-1,3-pentadiene-1,4-diyl     or 1-methyl-1,3-pentadiene-1,5-diyl; -   C₂-C₆-alkynediyl: ethyne-1,2-diyl, 1-propyne-1,3-diyl,     2-propyne-1,1-diyl, 2-propyne-1,3-diyl, 1-butyne-1,3-diyl,     1-butyne-1,4-diyl, 2-butyne-1,1-diyl, 2-butyne-1,4-diyl,     1-methyl-2-propyne-1,1-diyl, 1-methyl-2-propyne-1,3-diyl,     1-pentyne-1,3-diyl, 1-pentyne-1,4-diyl, 1-pentyne-1,5-diyl,     2-pentyne-1,1-diyl, 2-pentyne-1,4-diyl, 2-pentyne-1,5-diyl,     3-pentyne-1,1-diyl, 3-pentyne-1,2-diyl, 3-pentyne-1,5-diyl,     4-pentyne-1,1-diyl, 4-pentyne-1,2-diyl, 4-pentyne-1,3-diyl,     4-pentyne-1,5-diyl, 1-hexyne-1,3-diyl, 1-hexyne-1,4-diyl,     1-hexyne-1,5-diyl, 1-hexyne-1,6-diyl, 2-hexyne-1,1-diyl,     2-hexyne-1,4-diyl, 2-hexyne-1,5-diyl, 2-hexyne-1,6-diyl,     3-hexyne-1,1-diyl, 3-hexyne-1,2-diyl, 3-hexyne-1,5-diyl,     3-hexyne-1,6-diyl, 4-hexyne-1,1-diyl, 4-hexyne-1,2-diyl,     4-hexyne-1,3-diyl, 4-hexyne-1,6-diyl, 5-hexyne-1,1-diyl,     5-hexyne-1,2-diyl, 5-hexyne-1,3-diyl, 5-hexyne-1,4-diyl or     5-hexyne-1,6-diyl; -   C₃-C₆-cycloalkyl, and the cycloalkyl moieties of     C₃-C₆-cycloalkylamino and C₃-C₆-cycloalkylcarbonyl: for example     cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; -   aryl is understood as meaning carbocyclic aromatic compounds such as     phenyl or naphthyl; -   a 3- to 7-membered heterocycle is understood as meaning a saturated,     partially saturated or unsaturated 3-, 4-, 5-, 6- or 7-membered     heterocyclic ring which contains one, two, three or four identical     or different heteroatoms selected from the following group: oxygen,     sulfur or nitrogen, i.e., for example,

C-bonded 5-membered rings such as:

-   tetrahydrofuran-2-yl, tetrahydrofuran-3-yl, tetrahydrothien-2-yl,     tetrahydrothien-3-yl, tetrahydropyrrol-2-yl, tetrahydropyrrol-3-yl,     2,3-dihydrofuran-2-yl, 2,3-dihydrofuran-3-yl, 2,5-dihydrofuran-2-yl,     2,5-dihydrofuran-3-yl, 4,5-dihydrofuran-2-yl, 4,5-dihydrofuran-3-yl,     2,3-dihydrothien-2-yl, 2,3-dihydrothien-3-yl, 2,5-dihydrothien-2-yl,     2,5-dihydrothien-3-yl, 4,5-dihydrothien-2-yl, 4,5-dihydrothien-3-yl,     2,3-dihydro-1H-pyrrol-2-yl, 2,3-dihydro-1H-pyrrol-3-yl,     2,5-dihydro-1H-pyrrol-2-yl, 2,5-dihydro-1H-pyrrol-3-yl,     4,5-dihydro-1H-pyrrol-2-yl, 4,5-dihydro-1H-pyrrol-3-yl,     3,4-dihydro-2H-pyrrol-2-yl, 3,4-dihydro-2H-pyrrol-3-yl,     3,4-dihydro-5H-pyrrol-2-yl, 3,4-dihydro-5H-pyrrol-3-yl, 2-furyl,     3-furyl, 2-thienyl, 3-thienyl, pyrrol-2-yl, pyrrol-3-yl,     tetrahydropyrazol-3-yl, tetrahydropyrazol-4-yl,     tetrahydroisoxazol-3-yl, tetrahydroisoxazol-4-yl,     tetrahydroisoxazol-5-yl, 1,2-oxathiolan-3-yl, 1,2-oxathiolan-4-yl,     1,2-oxathiolan-5-yl, tetrahydroisothiazol-3-yl,     tetrahydroisothiazol-4-yl, tetrahydroisothiazol-5-yl,     1,2-dithiolan-3-yl, 1,2-dithiolan-4-yl, tetrahydroimidazol-2-yl,     tetrahydroimidazol-4-yl, tetrahydrooxazol-2-yl,     tetrahydrooxazol-4-yl, tetrahydrooxazol-5-yl,     tetrahydrothiazol-2-yl, tetrahydrothiazol-4-yl,     tetrahydrothiazol-5-yl, 1,3-dioxolan-2-yl, 1,3-dioxolan-4-yl,     1,3-oxathiolan-2-yl, 1,3-oxathiolan-4-yl, 1,3-oxathiolan-5-yl,     1,3-dithiolan-2-yl, 1,3-dithiolan-4-yl, 4,5-dihydro-1H-pyrazol-3-yl,     4,5-dihydro-1H-pyrazol-4-yl, 4,5-dihydro-1H-pyrazol-5-yl,     2,5-dihydro-1H-pyrazol-3-yl, 2,5-dihydro-1H-pyrazol-4-yl,     2,5-dihydro-1H-pyrazol-5-yl, 4,5-dihydroisoxazol-3-yl,     4,5-dihydroisoxazol-4-yl, 4,5-dihydroisoxazol-5-yl,     2,5-dihydroisoxazol-3-yl, 2,5-dihydroisoxazol-4-yl,     2,5-dihydroisoxazol-5-yl, 2,3-dihydroisoxazol-3-yl,     2,3-dihydroisoxazol-4-yl, 2,3-dihydroisoxazol-5-yl,     4,5-dihydroisothiazol-3-yl, 4,5-dihydroisothiazol-4-yl,     4,5-dihydroisothiazol-5-yl, 2,5-dihydroisothiazol-3-yl,     2,5-dihydroisothiazol-4-yl, 2,5-dihydroisothiazol-5-yl,     2,3-dihydroisothiazol-3-yl, 2,3-dihydroisothiazol-4-yl,     2,3-dihydroisothiazol-5-yl, Δ³-1,2-dithiol-3-yl,     Δ³-1,2-dithiol-4-yl, Δ³-1,2-dithiol-5-yl,     4,5-dihydro-1H-imidazol-2-yl, 4,5-dihydro-1H-imidazol-4-yl,     4,5-dihydro-1H-imidazol-5-yl, 2,5-dihydro-1H-imidazol-2-yl,     2,5-dihydro-1H-imidazol-4-yl, 2,5-dihydro-1H-imidazol-5-yl,     2,3-dihydro-1H-imidazol-2-yl, 2,3-dihydro-1H-imidazol-4-yl,     4,5-dihydrooxazol-2-yl, 4,5-dihydrooxazol-4-yl,     4,5-dihydrooxazol-5-yl, 2,5-dihydrooxazol-2-yl,     2,5-dihydrooxazol-4-yl, 2,5-dihydrooxazol-5-yl,     2,3-dihydrooxazol-2-yl, 2,3-dihydrooxazol-4-yl,     2,3-dihydrooxazol-5-yl, 4,5-dihydrothiazol-2-yl,     4,5-dihydrothiazol-4-yl, 4,5-dihydrothiazol-5-yl,     2,5-dihydrothiazol-2-yl, 2,5-dihydrothiazol-4-yl,     2,5-dihydrothiazol-5-yl, 2,3-dihydrothiazol-2-yl,     2,3-dihydrothiazol-4-yl, 2,3-dihydrothiazol-5-yl, 1,3-dioxol-2-yl,     1,3-dioxol-4-yl, 1,3-dithiol-2-yl, 1,3-dithiol-4-yl,     1,3-oxathiol-2-yl, 1,3-oxathiol-4-yl, 1,3-oxathiol-5-yl,     pyrazol-3-yl, pyrazol-4-yl, isoxazol-3-yl, isoxazol-4-yl,     isoxazol-5-yl, isothiazol-3-yl, isothiazol-4-yl, isothiazol-5-yl,     imidazol-2-yl, imidazol-4-yl, oxazol-2-yl, oxazol-4-yl, oxazol-5-yl,     thiazol-2-yl, thiazol-4-yl, thiazol-5-yl, 1,2,3-Δ²-oxadiazolin-4-yl,     1,2,3-Δ²-oxadiazolin-5-yl, 1,2,4-Δ⁴-oxadiazolin-3-yl,     1,2,4-Δ⁴-oxadiazolin-5-yl, 1,2,4-Δ²-oxadiazolin-3-yl,     1,2,4-Δ²-oxadiazolin-5-yl, 1,2,4-Δ³-oxadiazolin-3-yl,     1,2,4-Δ³-oxadiazolin-5-yl, 1,3,4-Δ²-oxadiazolin-2-yl,     1,3,4-Δ²-oxadiazolin-5-yl, 1,3,4-Δ³-oxadiazolin-2-yl,     1,3,4-oxadiazolin-2-yl, 1,2,4-Δ⁴-thiadiazolin-3-yl,     1,2,4-Δ⁴-thiadiazolin-5-yl, 1,2,4-Δ³-thiadiazolin-3-yl,     1,2,4-Δ³-thiadiazolin-5-yl, 1,2,4-Δ²-thiadiazolin-3-yl,     1,2,4-Δ²-thiadiazolin-5-yl, 1,3,4-Δ²-thiadiazolin-2-yl,     1,3,4-Δ²-thiadiazolin-5-yl, 1,3,4-Δ³-thiadiazolin-2-yl,     1,3,4-thiadiazolin-2-yl, 1,3,2-dioxathiolan-4-yl,     1,2,3-Δ²-triazolin-4-yl, 1,2,3-Δ²-triazolin-5-yl,     1,2,4-Δ²-triazolin-3-yl, 1,2,4-Δ²-triazolin-5-yl,     1,2,4-Δ³-triazolin-3-yl, 1,2,4-Δ³-triazolin-5-yl,     1,2,4-Δ¹-triazolin-2-yl, 1,2,4-triazolin-3-yl,     3H-1,2,4-dithiazol-5-yl, 2H-1,3,4-dithiazol-5-yl,     2H-1,3,4-oxathiazol-5-yl, 1,2,3-oxadiazol-4-yl,     1,2,3-oxadiazol-5-yl, 1,2,4-oxadiazol-3-yl, 1,2,4-oxadiazol-5-yl,     1,3,4-oxadiazol-2-yl, 1,2,3-thiadiazol-4-yl, 1,2,3-thiadiazol-5-yl,     1,2,4-thiadiazol-3-yl, 1,2,4-thiadiazol-5-yl, 1,3,4-thiadiazol-2-yl,     1,2,3-triazol-4-yl, 1,2,4-triazol-3-yl, tetrazol-5-yl;

C-bonded 6-membered rings such as:

-   tetrahydropyran-2-yl, tetrahydropyran-3-yl, tetrahydropyran-4-yl,     piperidin-2-yl, piperidin-3-yl, piperidin-4-yl,     tetrahydrothiopyran-2-yl, tetrahydrothiopyran-3-yl,     tetrahydrothiopyran-4-yl, 2H-3,4-dihydropyran-6-yl,     2H-3,4-dihydropyran-5-yl, 2H-3,4-dihydropyran-4-yl,     2H-3,4-dihydropyran-3-yl, 2H-3,4-dihydropyran-2-yl,     2H-3,4-dihydropyran-6-yl, 2H-3,4-dihydrothiopyran-5-yl,     2H-3,4-dihydrothiopyran-4-yl, 2H-3,4-dihydropyran-3-yl,     2H-3,4-dihydropyran-2-yl, 1,2,3,4-tetrahydropyridin-6-yl,     1,2,3,4-tetrahydropyridin-5-yl, 1,2,3,4-tetrahydropyridin-4-yl,     1,2,3,4-tetrahydropyridin-3-yl, 1,2,3,4-tetrahydropyridin-2-yl,     2H-5,6-dihydropyran-2-yl, 2H-5,6-dihydropyran-3-yl,     2H-5,6-dihydropyran-4-yl, 2H-5,6-dihydropyran-5-yl,     2H-5,6-dihydropyran-6-yl, 2H-5,6-dihydrothiopyran-2-yl,     2H-5,6-dihydrothiopyran-3-yl, 2H-5,6-dihydrothiopyran-4-yl,     2H-5,6-dihydrothiopyran-5-yl, 2H-5,6-dihydrothiopyran-6-yl,     1,2,5,6-tetrahydropyridin-2-yl, 1,2,5,6-tetrahydropyridin-3-yl,     1,2,5,6-tetrahydropyridin-4-yl, 1,2,5,6-tetrahydropyridin-5-yl,     1,2,5,6-tetrahydropyridin-6-yl, 2,3,4,5-tetrahydropyridin-2-yl,     2,3,4,5-tetrahydropyridin-3-yl, 2,3,4,5-tetrahydropyridin-4-yl,     2,3,4,5-tetrahydropyridin-5-yl, 2,3,4,5-tetrahydropyridin-6-yl,     4H-pyran-2-yl, 4H-pyran-3-yl, 4H-pyran-4-yl, 4H-thiopyran-2-yl,     4H-thiopyran-3-yl, 4H-thiopyran-4-yl, 1,4-dihydropyridin-2-yl,     1,4-dihydropyridin-3-yl, 1,4-dihydropyridin-4-yl, 2H-pyran-2-yl,     2H-pyran-3-yl, 2H-pyran-4-yl, 2H-pyran-5-yl, 2H-pyran-6-yl,     2H-thiopyran-2-yl, 2H-thiopyran-3-yl, 2H-thiopyran-4-yl,     2H-thiopyran-5-yl, 2H-thiopyran-6-yl, 1,2-dihydropyridin-2-yl,     1,2-dihydropyridin-3-yl, 1,2-dihydropyridin-4-yl,     1,2-dihydropyridin-5-yl, 1,2-dihydropyridin-6-yl,     3,4-dihydropyridin-2-yl, 3,4-dihydropyridin-3-yl,     3,4-dihydropyridin-4-yl, 3,4-dihydropyridin-5-yl,     3,4-dihydropyridin-6-yl, 2,5-dihydropyridin-2-yl,     2,5-dihydropyridin-3-yl, 2,5-dihydropyridin-4-yl,     2,5-dihydropyridin-5-yl, 2,5-dihydropyridin-6-yl,     2,3-dihydropyridin-2-yl, 2,3-dihydropyridin-3-yl,     2,3-dihydropyridin-4-yl, 2,3-dihydropyridin-5-yl,     2,3-dihydropyridin-6-yl, pyridin-2-yl, pyridin-3-yl, pyridin-4-yl,     1,3-dioxan-2-yl, 1,3-dioxan-4-yl, 1,3-dioxan-5-yl, 1,4-dioxan-2-yl,     1,3-dithian-2-yl, 1,3-dithian-4-yl, 1,3-dithian-5-yl,     1,4-dithian-2-yl, 1,3-oxathian-2-yl, 1,3-oxathian-4-yl,     1,3-oxathian-5-yl, 1,3-oxathian-6-yl, 1,4-oxathian-2-yl,     1,4-oxathian-3-yl, 1,2-dithian-3-yl, 1,2-dithian-4-yl,     hexahydropyrimidin-2-yl, hexahydropyrimidin-4-yl,     hexahydropyrimidin-5-yl, hexahydropyrazin-2-yl,     hexahydropyridazin-3-yl, hexahydropyridazin-4-yl,     tetrahydro-1,3-oxazin-2-yl, tetrahydro-1,3-oxazin-4-yl,     tetrahydro-1,3-oxazin-5-yl, tetrahydro-1,3-oxazin-6-yl,     tetrahydro-1,3-thiazin-2-yl, tetrahydro-1,3-thiazin-4-yl,     tetrahydro-1,3-thiazin-5-yl, tetrahydro-1,3-thiazin-6-yl,     tetrahydro-1,4-thiazin-2-yl, tetrahydro-1,4-thiazin-3-yl,     tetrahydro-1,4-oxazin-2-yl, tetrahydro-1,4-oxazin-3-yl,     tetrahydro-1,2-oxazin-3-yl, tetrahydro-1,2-oxazin-4-yl,     tetrahydro-1,2-oxazin-5-yl, tetrahydro-1,2-oxazin-6-yl,     2H-5,6-dihydro-1,2-oxazin-3-yl, 2H-5,6-dihydro-1,2-oxazin-4-yl,     2H-5,6-dihydro-1,2-oxazin-5-yl, 2H-5,6-dihydro-1,2-oxazin-6-yl,     2H-5,6-dihydro-1,2-thiazin-3-yl, 2H-5,6-dihydro-1,2-thiazin-4-yl,     2H-5,6-dihydro-1,2-thiazin-5-yl, 2H-5,6-dihydro-1,2-thiazin-6-yl,     4H-5,6-dihydro-1,2-oxazin-3-yl, 4H-5,6-dihydro-1,2-oxazin-4-yl,     4H-5,6-dihydro-1,2-oxazin-5-yl, 4H-5,6-dihydro-1,2-oxazin-6-yl,     4H-5,6-dihydro-1,2-thiazin-3-yl, 4H-5,6-dihydro-1,2-thiazin-4-yl,     4H-5,6-dihydro-1,2-thiazin-5-yl, 4H-5,6-dihydro-1,2-thiazin-6-yl,     2H-3,6-dihydro-1,2-oxazin-3-yl, 2H-3,6-dihydro-1,2-oxazin-4-yl,     2H-3,6-dihydro-1,2-oxazin-5-yl, 2H-3,6-dihydro-1,2-oxazin-6-yl,     2H-3,6-dihydro-1,2-thiazin-3-yl, 2H-3,6-dihydro-1,2-thiazin-4-yl,     2H-3,6-dihydro-1,2-thiazin-5-yl, 2H-3,6-dihydro-1,2-thiazin-6-yl,     2H-3,4-dihydro-1,2-oxazin-3-yl, 2H-3,4-dihydro-1,2-oxazin-4-yl,     2H-3,4-dihydro-1,2-oxazin-5-yl, 2H-3,4-dihydro-1,2-oxazin-6-yl,     2H-3,4-dihydro-1,2-thiazin-3-yl, 2H-3,4-dihydro-1,2-thiazin-4-yl,     2H-3,4-dihydro-1,2-thiazin-5-yl, 2H-3,4-dihydro-1,2-thiazin-6-yl,     2,3,4,5-tetrahydropyridazin-3-yl, 2,3,4,5-tetrahydropyridazin-4-yl,     2,3,4,5-tetrahydropyridazin-5-yl, 2,3,4,5-tetrahydropyridazin-6-yl,     3,4,5,6-tetrahydropyridazin-3-yl, 3,4,5,6-tetrahydropyridazin-4-yl,     1,2,5,6-tetrahydropyridazin-3-yl, 1,2,5,6-tetrahydropyridazin-4-yl,     1,2,5,6-tetrahydropyridazin-5-yl, 1,2,5,6-tetrahydropyridazin-6-yl,     1,2,3,6-tetrahydropyridazin-3-yl, 1,2,3,6-tetrahydropyridazin-4-yl,     4H-5,6-dihydro-1,3-oxazin-2-yl, 4H-5,6-dihydro-1,3-oxazin-4-yl,     4H-5,6-dihydro-1,3-oxazin-5-yl, 4H-5,6-dihydro-1,3-oxazin-6-yl,     4H-5,6-dihydro-1,3-thiazin-2-yl, 4H-5,6-dihydro-1,3-thiazin-4-yl,     4H-5,6-dihydro-1,3-thiazin-5-yl, 4H-5,6-dihydro-1,3-thiazin-6-yl,     3,4,5,6-tetrahydropyrimidin-2-yl, 3,4,5,6-tetrahydropyrimidin-4-yl,     3,4,5,6-tetrahydropyrimidin-5-yl, 3,4,5,6-tetrahydropyrimidin-6-yl,     1,2,3,4-tetrahydropyrazin-2-yl, 1,2,3,4-tetrahydropyrazin-5-yl,     1,2,3,4-tetrahydropyrimidin-2-yl, 1,2,3,4-tetrahydropyrimidin-4-yl,     1,2,3,4-tetrahydropyrimidin-5-yl, 1,2,3,4-tetrahydropyrimidin-6-yl,     2,3-dihydro-1,4-thiazin-2-yl, 2,3-dihydro-1,4-thiazin-3-yl,     2,3-dihydro-1,4-thiazin-5-yl, 2,3-dihydro-1,4-thiazin-6-yl,     2H-1,2-oxazin-3-yl, 2H-1,2-oxazin-4-yl, 2H-1,2-oxazin-5-yl,     2H-1,2-oxazin-6-yl, 2H-1,2-thiazin-3-yl, 2H-1,2-thiazin-4-yl,     2H-1,2-thiazin-5-yl, 2H-1,2-thiazin-6-yl, 4H-1,2-oxazin-3-yl,     4H-1,2-oxazin-4-yl, 4H-1,2-oxazin-5-yl, 4H-1,2-oxazin-6-yl,     4H-1,2-thiazin-3-yl, 4H-1,2-thiazin-4-yl, 4H-1,2-thiazin-5-yl,     4H-1,2-thiazin-6-yl, 6H-1,2-oxazin-3-yl, 6H-1,2-oxazin-4-yl,     6H-1,2-oxazin-5-yl, 6H-1,2-oxazin-6-yl, 6H-1,2-thiazin-3-yl,     6H-1,2-thiazin-4-yl, 6H-1,2-thiazin-5-yl, 6H-1,2-thiazin-6-yl,     2H-1,3-oxazin-2-yl, 2H-1,3-oxazin-4-yl, 2H-1,3-oxazin-5-yl,     2H-1,3-oxazin-6-yl, 2H-1,3-thiazin-2-yl, 2H-1,3-thiazin-4-yl,     2H-1,3-thiazin-5-yl, 2H-1,3-thiazin-6-yl, 4H-1,3-oxazin-2-yl,     4H-1,3-oxazin-4-yl, 4H-1,3-oxazin-5-yl, 4H-1,3-oxazin-6-yl,     4H-1,3-thiazin-2-yl, 4H-1,3-thiazin-4-yl, 4H-1,3-thiazin-5-yl,     4H-1,3-thiazin-6-yl, 6H-1,3-oxazin-2-yl, 6H-1,3-oxazin-4-yl,     6H-1,3-oxazin-5-yl, 6H-1,3-oxazin-6-yl, 6H-1,3-thiazin-2-yl,     6H-1,3-oxazin-4-yl, 6H-1,3-oxazin-5-yl, 6H-1,3-thiazin-6-yl,     2H-1,4-oxazin-2-yl, 2H-1,4-oxazin-3-yl, 2H-1,4-oxazin-5-yl,     2H-1,4-oxazin-6-yl, 2H-1,4-thiazin-2-yl, 2H-1,4-thiazin-3-yl,     2H-1,4-thiazin-5-yl, 2H-1,4-thiazin-6-yl, 4H-1,4-oxazin-2-yl,     4H-1,4-oxazin-3-yl, 4H-1,4-thiazin-2-yl, 4H-1,4-thiazin-3-yl,     1,4-dihydropyridazin-3-yl, 1,4-dihydropyridazin-4-yl,     1,4-dihydropyridazin-5-yl, 1,4-dihydropyridazin-6-yl,     1,4-dihydropyrazin-2-yl, 1,2-dihydropyrazin-2-yl,     1,2-dihydropyrazin-3-yl, 1,2-dihydropyrazin-5-yl,     1,2-dihydropyrazin-6-yl, 1,4-dihydropyrimidin-2-yl,     1,4-dihydropyrimidin-4-yl, 1,4-dihydropyrimidin-5-yl,     1,4-dihydropyrimidin-6-yl, 3,4-dihydropyrimidin-2-yl,     3,4-dihydropyrimidin-4-yl, 3,4-dihydropyrimidin-5-yl,     3,4-dihydropyrimidin-6-yl, pyridazin-3-yl, pyridazin-4-yl,     pyrimidin-2-yl, pyrimidin-4-yl, pyrimidin-5-yl, pyrazin-2-yl,     1,3,5-triazin-2-yl, 1,2,4-triazin-3-yl, 1,2,4-triazin-5-yl,     1,2,4-triazin-6-yl or 1,2,4,5-tetrazin-3-yl;

N-bonded 5-membered rings such as:

-   tetrahydropyrrol-1-yl, 2,3-dihydro-1H-pyrrol-1-yl,     2,5-dihydro-1H-pyrrol-1-yl, pyrrol-1-yl, tetrahydropyrazol-1-yl,     tetrahydroisoxazol-2-yl, tetrahydroisothiazol-2-yl,     tetrahydroimidazol-1-yl, tetrahydrooxazol-3-yl,     tetrahydrothiazol-3-yl, 4,5-dihydro-1H-pyrazol-1-yl,     2,5-dihydro-1H-pyrazol-1-yl, 2,3-dihydro-1H-pyrazol-1-yl,     2,5-dihydroisoxazol-2-yl, 2,3-dihydroisoxazol-2-yl,     2,5-dihydroisothiazol-2-yl, 2,3-dihydroisoxazol-2-yl,     4,5-dihydro-1H-imidazol-1-yl, 2,5-dihydro-1H-imidazol-1-yl,     2,3-dihydro-1H-imidazol-1-yl, 2,3-dihydrooxazol-3-yl,     2,3-dihydrothiazol-3-yl, pyrazol-1-yl, imidazol-1-yl,     1,2,4-Δ⁴-oxadiazolin-2-yl, 1,2,4-Δ²-oxadiazolin-4-yl,     1,2,4-Δ³-oxadiazolin-2-yl, 1,3,4-Δ²-oxadiazolin-4-yl,     1,2,4-Δ⁵-thiadiazolin-2-yl, 1,2,4-Δ³-thiadiazolin-2-yl,     1,2,4-Δ²-thiadiazolin-4-yl, 1,3,4-Δ²-thiadiazolin-4-yl,     1,2,3-Δ²-triazolin-1-yl, 1,2,4-Δ²-triazolin-1-yl,     1,2,4-Δ²-triazolin-4-yl, 1,2,4-Δ³-triazolin-1-yl,     1,2,4-Δ¹-triazolin-4-yl, 1,2,3-triazol-1-yl, 1,2,4-triazol-1-yl,     tetrazol-1-yl;

N-bonded 6-membered rings such as:

-   piperidin-1-yl, 1,2,3,4-tetrahydropyridin-1-yl,     1,2,5,6-tetrahydropyridin-1-yl, 1,4-dihydropyridin-1-yl,     1,2-dihydropyridin-1-yl, hexahydropyrimidin-1-yl,     hexahydropyrazin-1-yl, hexahydropyridazin-1-yl,     tetrahydro-1,3-oxazin-3-yl, tetrahydro-1,3-thiazin-3-yl,     tetrahydro-1,4-thiazin-4-yl, tetrahydro-1,4-oxazin-4-yl     (morpholinyl), tetrahydro-1,2-oxazin-2-yl,     2H-5,6-dihydro-1,2-oxazin-2-yl, 2H-5,6-dihydro-1,2-thiazin-2-yl,     2H-3,6-dihydro-1,2-oxazin-2-yl, 2H-3,6-dihydro-1,2-thiazin-2-yl,     2H-3,4-dihydro-1,2-thiazin-2-yl, 2,3,4,5-tetrahydropyridazin-2-yl,     1,2,5,6-tetrahydropyridazin-1-yl, 1,2,5,6-tetrahydropyridazin-2-yl,     1,2,3,6-tetrahydropyridazin-1-yl, 3,4,5,6-tetrahydropyrimidin-3-yl,     1,2,3,4-tetrahydropyrazin-1-yl, 1,2,3,4-tetrahydropyrimidin-1-yl,     1,2,3,4-tetrahydropyrimidin-3-yl, 2,3-dihydro-1,4-thiazin-4-yl,     2H-1,2-oxazin-2-yl, 2H-1,2-thiazin-2-yl, 4H-1,4-oxazin-4-yl,     4H-1,4-thiazin-4-yl, 1,4-dihydropyridazin-1-yl,     1,4-dihydropyrazin-1-yl, 1,2-dihydropyrazin-1-yl,     1,4-dihydropyrimidin-1-yl or 3,4-dihydropyrimidin-3-yl;

and also N-bonded cyclic imides such as:

-   phthalimide, tetrahydrophthalimide, succinimide, maleimide,     glutarimide, 5-oxotriazolin-1-yl, 5-oxo-1,3,4-oxadiazolin-4-yl or     2,4-dioxo(1H,3H)pyrimidin-3-yl; -   where, if appropriate, the sulfur of the heterocycles mentioned may     be oxidized to S═O or S(═O)₂ -   and where a bicyclic ring system may be formed with a fused-on     phenyl ring or with a C₃-C₆-carbocycle or with a further 5- to     6-membered heterocycle.

All phenyl rings or heterocyclyl radicals and all phenyl components in phenoxy, phenylalkyl, phenylcarbonylalkyl, phenylcarbonyl, phenylalkenylcarbonyl, phenoxycarbonyl, phenyloxythiocarbonyl, phenylaminocarbonyl and N-alkyl-N-phenylaminocarbonyl, phenylsulfonyl or phenoxysulfonyl or heterocyclyl components in heterocyclyloxy, heterocyclylalkyl, heterocyclylcarbonylalkyl, heterocyclylcarbonyl, heterocyclyloxythiocarbonyl, heterocyclylalkenylcarbonyl, heterocyclyloxycarbonyl, heterocyclylaminocarbonyl, N-alkyl-N-heterbcyclylaminocarbonyl, heterocyclylsulfonyl or heterocyclyloxysulfonyl are, unless stated otherwise, preferably unsubstituted, or they carry one, two or three halogen atoms and/or a nitro group, a cyano radical and/or one or two methyl, trifluoromethyl, methoxy or trifluoromethoxy substituents.

With respect to the use of the compounds of the formula I according to the invention as herbicides, the variables A, R¹ to R¹⁹ preferably have the following meanings, in each case on their own or in combination:

-   A is O or NR⁶, where R⁶ is as defined above. R⁶ is preferably not     hydrogen. R⁶ is in particular C₁-C₄-alkyl and very particularly     preferably methyl. Another preferred class of the compounds I are     those where A is S. -   R¹ is halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, in particular methyl,     methoxy or chlorine. -   R² has the abovementioned meanings other than hydrogen, and is in     particular C₁-C₄-alkyl, C₁-C₄-haloalkyl, hydroxyl, C₁-C₄-alkoxy,     C₁-C₄-alkylsulfonyl, C₁-C₄-haloalkylsulfonyl, hydroxycarbonyl-C     ₁-C₄-alkyl, C(═N—O(—C₁-C₄-alkyl))-(C₁-C₄-alkyl), NH₂,     C₁-C₄-alkylamino, di(C₁-C₄-alkyl)amino, phenyl, phenylcarbonyl or     benzyl, where the phenyl rings of the three lastmentioned     substituents may be substituted by one or two halogen atoms, methoxy     groups or methyl groups, cyano, C₁-C₄-alkylcarbonyl,     C₁-C₄-haloalkylcarbonyl, C₁-C₄-alkoxycarbonyl,     C₁-C₄-alkoxycarbonyl-C₁-C₄-alkyl, C₃-C₆-alkenyl, C₃-C₆-alkynyl,     1,3-dioxolan-2-yl, 1,3-dithiolan-2-yl, 1,3-dioxan-2-yl,     1,3-dithian-2-yl, oxazolin-2-yl, oxazolidin-2-yl,     4,5-dihydroisoxazol-3-yl, 4,5-dihydroisoxazol-4-yl, isoxazol-3-yl,     isoxazol-4-yl, methyl or ethyl substituted by one of the     heterocycles mentioned above, such as in (1,3-dioxolan-2-yl)methyl,     (1,3-dithiolan-2-yl)methyl, (1,3-dioxan-2-yl)methyl,     (1,3-dithian-2-yl)methyl, (oxazolin-2-yl)methyl,     (oxazolidin-2-yl)methyl, (4,5-dihydroisoxazol-3-yl)methyl,     (4,5-dihydroisoxazol-4-yl)methyl, (isoxazol-3-yl)methyl,     (isoxazol-4-yl)methyl, 2-(1,3-dioxolan-2-yl)ethyl,     2-(1,3-dithiolan-2-yl)ethyl, 2-(1,3-dioxan-2-yl)ethyl,     2-(1,3-dithian-2-yl)ethyl, 2-(oxazolin-2-yl)ethyl,     2-(oxazolidin-2-yl)ethyl, 2-(4,5-dihydroisoxazol-3-yl)ethyl,     (4,5-dihydroisoxazol-4-yl)ethyl, 2-(isoxazol-3-yl)ethyl,     2-(isoxazol-4-yl)ethyl, where the abovementioned heterocycles may be     mono-, di- or trisubstituted by C₁-C₄-alkyl, in particular methyl;     and is especially C₁-C₄-alkyl, C₃-C₆-alkenyl, methoxymethyl, CF₃,     CHF₂, CN, OH, OCH₃, NH₂, NHCH₃, N(CH₃)₂, C₁-C₄-alkoxy-carbonyl,     acetyl, trifluoroacetyl, C(═NOCH₃) CH₃, SO₂CH₃, SO₂CF₃, CH₂CO₂H,     C₁-C₄-alkoxycarbonyl-C₁-C₄-alkyl, cyclopropyl, cyclopentyl,     cyclohexyl, 4,5-dihydroisoxazol-3-yl, 4,5-dihydroisoxazol-4-yl,     isoxazol-3-yl, isoxazol-4-yl, where the abovementioned heterocycles     may be monosubstituted by methyl, is phenyl, benzyl, benzoyl,     2-pyridyl. -    R² is particularly preferably C₁-C₆-alkyl or C₃-C₆-alkenyl.     Particular preference is also given to those compounds I in which R²     is C₃-C₆-alkynyl, (1,3-dioxolan-2-yl)methyl,     2-(1,3-dioxolan-2-yl)ethyl or benzyl where the phenyl ring may be     unsubstituted or carry 1 or 2 substituents, selected from the group     consisting of halogen, methyl and methoxy. -   R³ is C₁-C₄-alkyl, halogen and in particular hydrogen.

In very particularly prefered compounds I, A is O or S, R¹ is methyl, R³ is hydrogen and R³ is a substituent different from hydrogen, in particular one of the substituents mentioned above as being preferred and specifically C₁-C₆-alkyl, C₃-C₆-alkynyl, C₃-C₆-alkenyl, (1,3-dioxolan-2-yl)methyl, 2-(1,3-dioxolan-2-yl)ethyl or benzyl where the phenyl ring may be unsubstituted or may carry 1 or 2 substituents selected from the group consisting of halogen, methyl and methoxy.

-   R⁷, R⁸, R⁹, R¹⁰, R¹¹, R¹² and R¹³ preferably have the following     meanings: -   R⁷ is hydroxyl, halogen, mercapto, OR¹⁴, SR¹⁴, SO₂R¹⁵, OSO₂R¹⁵,     NR¹⁸R¹⁹, ONR¹⁸R¹⁹ or N-bonded heterocyclyl, such as pyrrolidinyl,     piperidinyl, morpholinyl, pyrazolinyl or imidazolidinyl, which may     be partially or fully halogenated and/or may carry one, two or three     of the following radicals: nitro, cyano, C₁-C₄-alkyl,     C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy; in particular     hydroxyl, OR¹⁴, SR¹⁴, N(OR¹⁸)R¹⁹; particularly preferably hydroxyl,     C₁-C₄-alkyloxy, C₁-C₄-alkylamino, di-C₁-C₄-alkylamino,     N-C₁-C₄-alkoxy-C₁-C₄-alkylamino, C₁-C₄-alkylthio, phenylthio,     O—CH₂-phenyl, phenylcarbonyloxy, 2-, 3- or     4-fluorophenylcarbonyloxy, C₁-C₄-sulfonyloxy, phenylsulfonyloxy and     2-, 3- or 4-methylphenylsulfonyloxy; -   R⁸, R¹² are hydrogen or C₁-C₄-alkyl, such as methyl, ethyl or     propyl; -    preferably hydrogen or methyl; -   R⁹, R¹¹, R¹³ are hydrogen or C₁-C₄-alkyl, such as methyl, ethyl or     propyl; -    preferably hydrogen or methyl; -   R¹⁰ is hydrogen, hydroxyl, C₁-C₆-alkyl, di-C₁-C₆-alkoxy)methyl,     (C₁-C₆-alkoxy)-(C₁-C₅-alkylthio)methyl, di-(C₁-C₆-alkylthio)methyl,     C₁-C₆-alkylthio, C₁-C₆-haloalkylthio, C₁-C₆-alkylsulfinyl,     C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl or     C₁-C₆-haloalkylsulfonyl; -    is 1,3-dioxolan-2-yl, 1,3-dioxan-2-yl, 1,3-oxathiolan-2-yl,     1,3-oxathian-2-yl, 1,3-dithiolan-2-yl or 1,3-dithian-2-yl, where the     six lastmentioned radicals may be substituted by one, two or three     C₁-C₄-alkyl radicals;     -   preferably hydrogen, hydroxyl or C₁-C₄-alkyl, such as methyl,         ethyl or propyl; -   or -   R⁹ and R¹¹ or R¹¹ and R¹³ together form a n bond or a C₃-C₅-alkyl     chain which may carry one to three radicals from the following     group: halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl or     C₁-C₄-alkoxycarbonyl; -   or -   R⁹ and R¹³ or R⁸ and R¹² together form a C₁-C₄-alkyl chain which may     carry one to three radicals from the following group: halogen,     cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl or C₁-C₄-alkoxycarbonyl; -   or -   R¹⁰ and R¹¹ together form a —O—(CH₂)_(p)—O—,—O—(CH₂)_(p)—S— or     —S—(CH₂)_(p)—S— chain which may be substituted by one to three     radicals from the following group: halogen, cyano, C₁-C₄-alkyl,     C₁-C₄-haloalkyl or C₁-C₄-alkoxycarbonyl; -   or -   R¹⁰ and R¹¹ together preferably form a —O—(CH₂)_(p)—O—,     —O—(CH₂)_(p)—S— or —S—(CH₂)_(p)—S— chain which may be substituted by     one to three radicals from the following group: C₁-C₄-haloalkyl or     C₁-C₄-alkoxycarbonyl; -   or -   R¹⁰ and R₁₁ together with the carbons to which they are attached     form a carbonyl group. The variable p is preferably 2 or 3 and the     variable q is preferably 2, 3 or 4.

Preferred meanings of R¹⁴ to R¹⁹ are:

-   R¹⁴ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-alkynyl,     C₁-C₆-alkylcarbonyl, C₂-C₆-alkenylcarbonyl,     C₃-C₆-cycloalkylcarbonyl, C₁-C₆-alkoxycarbonyl,     C₃-C₆-alkenyloxycarbonyl, C₃-C₆-alkynyloxycarbonyl,     C₁-C₆-alkylthiocarbonyl, C₁-C₆-alkylaminocarbonyl,     C₃-C₆-alkenylaminocarbonyl, C₃-C₆-alkynylaminocarbonyl,     N,N-di(C₁-C₆-alkyl)aminocarbonyl,     N-(C₃-C₆-alkenyl)-N-(C₁-C₆-alkyl)aminocarbonyl,     N-(C₃-C₆-alkynyl)-N-(C₁-C₆-alkyl)aminocarbonyl,     N-(C₁-C₆-alkoxy)-N-(C₁-C₆-alkyl)aminocarbonyl,     N-(C₃-C₆-alkenyl)-N-(C₁-C₆-alkoxy)aminocarbonyl,     N-(C₃-C₆-alkynyl)-N-(C₁-C₆-alkoxy)aminocarbonyl,     di-(C₁-C₆-alkyl)aminothiocarbonyl, C₁-C₆-alkoxyimino-C₁-C₆-alkyl,     where the alkyl, cycloalkyl or alkoxy radicals mentioned may be     partially or fully halogenated and/or may carry one to three of the     following groups: cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio,     di-(C₁-C₄-alkyl)amino, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl,     hydroxycarbonyl, C₁-C₄-alkylaminocarbonyl,     di-(C₁-C₄-alkyl)aminocarbonyl, C₁-C₄-alkylcarbonyloxy or     C₃-C₆-cycloalkyl; -    is phenyl, phenyl-C₁-C₆-alkyl, phenylcarbonyl-C₁-C₆-alkyl,     phenylcarbonyl, phenoxycarbonyl, phenoxythiocarbonyl,     phenyl-C₂-C₆-alkenylcarbonyl, heterocyclyl,     heterocyclyl-C₁-C₆-alkyl, heterocyclylcarbonyl-C₁-C₆-alkyl,     heterocyclylcarbonyl, heterocyclyloxy-carbonyl,     heterocyclyloxythiocarbonyl or heterocyclyl-C₁-C₆-alkenylcarbonyl,     where the phenyl or the heterocyclyl radical of the 14 lastmentioned     substituents may be partially or fully halogenated and/or may carry     one to three of the following radicals: nitro, cyano, C₁-C₄-alkyl,     C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy; -    preferably C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-alkynyl,     C₁-C₆-alkylcarbonyl, C₁-C₆-alkoxycarbonyl, C₁-C₆-alkylaminocarbonyl     or N,N-di(C₁-C₆-alkyl)aminocarbonyl, where the alkyl or alkoxy     radicals mentioned may be partially or fully halogenated and/or may     carry one to three of the following groups: cyano, C₁-C₄-alkoxy,     C₁-C₄-alkylthio or C₁-C₄-alkoxycarbonyl; -    phenyl, phenyl-C₁-C₆-alkyl, phenylcarbonyl-C₁-C₆-alkyl,     phenylcarbonyl, phenoxycarbonyl, heterocyclyl,     heterocyclyl-C₁-C₆-alkyl, heterocyclylcarbonyl-C₁-C₆-alkyl,     heterocyclylcarbonyl or heterocyclyloxycarbonyl, where the phenyl or     the heterocyclyl radical of the 10 lastmentioned substituents may be     partially or fully halogenated and/or may carry one to three of the     following radicals: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl,     C₁-C₄-alkoxy or C₁-C₄-haloalkoxy; -   R¹⁵ is C₁-C₆-alkyl, C₃-C₆-alkenyl or C₃-C₆-cycloalkyl, where the     three radicals mentioned may be partially or fully halogenated     and/or may carry one to three of the following groups: cyano,     C₁-C₄-alkoxy, C₁-C₄-alkylthio, C₁-C₄-alkylcarbonyl or     C₁-C₄-alkoxycarbonyl; -    is phenyl, phenyl-C₁-C₄-alkyl, heterocyclyl or     heterocyclyl-C₁-C₄-alkyl, where the phenyl or the heterocyclyl     radical of the four lastmentioned substituents may be partially or     fully halogenated and/or may carry one to three of the following     radicals: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy,     C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl; -   R¹⁶, R¹⁷ are hydroxyl, C₁-C₆-alkyl, C₁-C₆-alkoxy, phenyl,     phenyl-C₁-C₄-alkyl or phenoxy, where the three lastmentioned     substituents may be partially or fully halogenated and/or may carry     one to three of the following radicals: nitro, cyano, C₁-C₄-alkyl,     C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or     C₁-C₄-alkoxycarbonyl; -   R¹⁸ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-halogenalkenyl,     C₃-C₆-cycloalkyl, C₁-C₆-alkoxy, C₃-C₆-alkenyloxy or     di-(C₁-C₆-alkyl)amino, where the alkyl, cycloalkyl or alkoxy     radicals mentioned may be partially or fully halogenated and/or may     carry one to three of the following radicals: cyano,     C₁-C₄-alkoxycarbonyl, C₁-C₄-alkylaminocarbonyl,     di-(C₁-C₄-alkyl)aminocarbonyl or C₃-C₆-cycloalkyl; -    is phenyl, phenyl-C₁-C₄-alkyl, phenylcarbonyl, heterocyclyl,     heterocyclyl-C₁-C₄-alkyl or heterocyclylcarbonyl, where the phenyl     or heterocyclyl radical of the six lastmentioned substituents may be     partially or fully halogenated and/or may carry one to three of the     following radicals: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl,     C₁-C₄-alkoxy or C₁-C₄-haloalkoxy; -   R¹⁹ is C₁-C₆-alkyl or C₃-C₆-alkenyl.

Preference is given to compounds of the formula I in which Hexk is a compound of the formula IIa or IIb″.

Examples of preferred radicals Hex have the formulae IIa-1 to IIa-8.

where the OH group in these radicals may also be replaced by one of the following groups: O—CH₃, N(CH₃)₂, N(OCH₃)CH₃, pyrrolidinyl, piperidinyl, morpholinyl, imidazolinyl, pyrazolinyl or S-phenyl. A particularly preferred group of the compounds I has a radical Hex of the formula IIa-4.

Examples of preferred compounds of the formula I are the benzazolonylcarbonylcyclohexenones I listed in Tables 1 to 25 below, where A, R¹, R² and R³ in each case have the meanings given in one row of the table.

TABLE A No. R¹ R² R³ A 1 CH₃ H H O 2 CH₃ CH₃ H O 3 CH₃ C₂H₅ H O 4 CH₃ n-C₃H₇ H O 5 CH₃ i-C₃H₇ H O 6 CH₃ n-C₄H₉ H O 7 CH₃ i-C₄H₉ H O 8 CH₃ s-C₄H₉ H O 9 CH₃ t-C₄H₉ H O 10 CH₃ CH₂OCH₃ H O 11 CH₃ CF₃ H O 12 CH₃ CF₂H H O 13 CH₃ CN H O 14 CH₃ OH H O 15 CH₃ OCH₃ H O 16 CH₃ NH₂ H O 17 CH₃ NHCH₃ H O 18 CH₃ N(CH₃)₂ H O 19 CH₃ CO₂CH₃ H O 20 CH₃ CO₂C₂H₅ H O 21 CH₃ C(O)CH₃ H O 22 CH₃ C(O)CF₃ H O 23 CH₃ C(═NOCH₃)CH₃ H O 24 CH₃ SO₂CH₃ H O 25 CH₃ SO₂CF₃ H O 26 CH₃ CH₂CO₂H H O 27 CH₃ CH₂COOCH₃ H O 28 CH₃ CH₂COOC₂H₅ H O 29 CH₃ prop-1-en-3-yl H O 30 CH₃ trans-but-2-en-1-yl H O 31 CH₃ cis-but-2-en-1-yl H O 32 CH₃ cis-3-methyl- H O but-2-en-1-yl 33 CH₃ cyclopropyl H O 34 CH₃ cyclopentyl H O 35 CH₃ cyclohexyl H O 36 CH₃ 4,5-dihydroisoxazol- H O 3-yl 37 CH₃ 4-methyl-4,5-dihydro- H O isoxazol-3-yl 38 CH₃ isoxazol-3-yl H O 39 CH₃ 4-methylisoxazol-3-yl H O 40 CH₃ 4,5-dihydroisoxazol- H O 4-yl 41 CH₃ 3-methyl-4,5-dihydro- H O isoxazol-4-yl 42 CH₃ isoxazol-4-yl H O 43 CH₃ 3-methylisoxazol-4-yl H O 44 CH₃ phenyl H O 45 CH₃ benzyl H O 46 CH₃ benzoyl H O 47 CH₃ 2-pyridyl H O 48 CH₃ H CH₃ O 49 CH₃ CH₃ CH₃ O 50 CH₃ C₂H₅ CH₃ O 51 CH₃ n-C₃H₇ CH₃ O 52 CH₃ i-C₃H₇ CH₃ O 53 CH₃ n-C₄H₉ CH₃ O 54 CH₃ i-C₄H₉ CH₃ O 55 CH₃ s-C₄H₉ CH₃ O 56 CH₃ t-C₄H₉ CH₃ O 57 CH₃ CH₂OCH₃ CH₃ O 58 CH₃ CF₃ CH₃ O 59 CH₃ CF₂H CH₃ O 60 CH₃ CN CH₃ O 61 CH₃ OH CH₃ O 62 CH₃ OCH₃ CH₃ O 63 CH₃ NH₂ CH₃ O 64 CH₃ NHCH₃ CH₃ O 65 CH₃ N(CH₃)₂ CH₃ O 66 CH₃ CO₂CH₃ CH₃ O 67 CH₃ CO₂C₂H₅ CH₃ O 68 CH₃ C(O)CH₃ CH₃ O 69 CH₃ C(O)CF₃ CH₃ O 70 CH₃ C(═NOCH₃)CH₃ CH₃ O 71 CH₃ SO₂CH₃ CH₃ O 72 CH₃ SO₂CF₃ CH₃ O 73 CH₃ CH₂CO₂H CH₃ O 74 CH₃ CH₂COOCH₃ CH₃ O 75 CH₃ CH₂COOC₂H₅ CH₃ O 76 CH₃ prop-1-en-3-yl CH₃ O 77 CH₃ trans-but-2-en-1-yl CH₃ O 78 CH₃ cis-but-2-en-1-yl CH₃ O 79 CH₃ cis-3-methyl- CH₃ O but-2-en-1-yl 80 CH₃ cyclopropyl CH₃ O 81 CH₃ cyclopentyl CH₃ O 82 CH₃ cyclohexyl CH₃ O 83 CH₃ 4,5-dihydroisoxazol- CH₃ O 3-yl 84 CH₃ 4-methyl-4,5-dihydro- CH₃ O isoxazol-3-yl 85 CH₃ isoxazol-3-yl CH₃ O 86 CH₃ 4-methylisoxazol-3-yl CH₃ O 87 CH₃ 4,5-dihydroisoxazol- CH₃ O 4-yl 88 CH₃ 3-methyl-4,5-dihydro- CH₃ O isoxazol-4-yl 89 CH₃ isoxazol-4-yl CH₃ O 90 CH₃ 3-methylisoxazol-4-yl CH₃ O 91 CH₃ phenyl CH₃ O 92 CH₃ benzyl CH₃ O 93 CH₃ benzoyl CH₃ O 94 CH₃ 2-pyridyl CH₃ O 95 CH₃ H Cl O 96 CH₃ CH₃ Cl O 97 CH₃ C₂H₅ Cl O 98 CH₃ n-C₃H₇ Cl O 99 CH₃ i-C₃H₇ Cl O 100 CH₃ n-C₄H₉ Cl O 101 CH₃ i-C₄H₉ Cl O 102 CH₃ s-C₄H₉ Cl O 103 CH₃ t-C₄H₉ Cl O 104 CH₃ CH₂OCH₃ Cl O 105 CH₃ CF₃ Cl O 106 CH₃ CF₂H Cl O 107 CH₃ CN Cl O 108 CH₃ OH Cl O 109 CH₃ OCH₃ Cl O 110 CH₃ NH₂ Cl O 111 CH₃ NHCH₃ Cl O 112 CH₃ N(CH₃)₂ Cl O 113 CH₃ CO₂CH₃ Cl O 114 CH₃ CO₂C₂H₅ Cl O 115 CH₃ C(O)CH₃ Cl O 116 CH₃ C(O)CF₃ Cl O 117 CH₃ C(═NOCH₃)CH₃ Cl O 118 CH₃ SO₂CH₃ Cl O 119 CH₃ SO₂CF₃ Cl O 120 CH₃ CH₂CO₂H Cl O 121 CH₃ CH₂COOCH₃ Cl O 122 CH₃ CH₂COOC₂H₅ Cl O 123 CH₃ prop-1-en-3-yl Cl O 124 CH₃ trans-but-2-en-1-yl Cl O 125 CH₃ cis-but-2-en-1-yl Cl O 126 CH₃ cis-3-methyl- Cl O but-2-en-1-yl 127 CH₃ cyclopropyl Cl O 128 CH₃ cyclopentyl Cl O 129 CH₃ cyclohexyl Cl O 130 CH₃ 4,5-dihydroisoxazol- Cl O 3-yl 131 CH₃ 4-methyl-4,5-dihydro- Cl O isoxazol-3-yl 132 CH₃ isoxazol-3-yl Cl O 133 CH₃ 4-methylisoxazol-3-yl Cl O 134 CH₃ 4,5-dihydroisoxazol- Cl O 4-yl 135 CH₃ 3-methyl-4,5-dihydro- Cl O isoxazol-4-yl 136 CH₃ isoxazol-4-yl Cl O 137 CH₃ 3-methylisoxazol-4-yl Cl O 138 CH₃ phenyl Cl O 139 CH₃ benzyl Cl O 140 CH₃ benzoyl Cl O 141 CH₃ 2-pyridyl Cl O 142 Cl H H O 143 Cl CH₃ H O 144 Cl C₂H₅ H O 145 Cl n-C₃H₇ H O 146 Cl i-C₃H₇ H O 147 Cl n-C₄H₉ H O 148 Cl i-C₄H₉ H O 149 Cl s-C₄H₉ H O 150 Cl t-C₄H₉ H O 151 Cl CH₂OCH₃ H O 152 Cl CF₃ H O 153 Cl CF₂H H O 154 Cl CN H O 155 Cl OH H O 156 Cl OCH₃ H O 157 Cl NH₂ H O 158 Cl NHCH₃ H O 159 Cl N(CH₃)₂ H O 160 Cl CO₂CH₃ H O 161 Cl CO₂C₂H₅ H O 162 Cl C(O)CH₃ H O 163 Cl C(O)CF₃ H O 164 Cl C(═NOCH₃)CH₃ H O 165 Cl SO₂CH₃ H O 166 Cl SO₂CF₃ H O 167 Cl CH₂CO₂H H O 168 Cl CH₂COOCH₃ H O 169 Cl CH₂COOC₂H₅ H O 170 Cl prop-1-en-3-yl H O 171 Cl trans-but-2-en-1-yl H O 172 Cl cis-but-2-en-1-yl H O 173 Cl cis-3-methyl- H O but-2-en-1-yl 174 Cl cyclopropyl H O 175 Cl cyclopentyl H O 176 Cl cyclohexyl H O 177 Cl 4,5-dihydroisoxazol- H O 3-yl 178 Cl 4-methyl-4,5-dihydro- H O isoxazol-3-yl 179 Cl isoxazol-3-yl H O 180 Cl 4-methylisoxazol-3-yl H O 181 Cl 4,5-dihydroisoxazol- H O 4-yl 182 Cl 3-methyl-4,5-dihydro- H O isoxazol-4-yl 183 Cl isoxazol-4-yl H O 184 Cl 3-methylisoxazol-4-yl H O 185 Cl phenyl H O 186 Cl benzyl H O 187 Cl benzoyl H O 188 Cl 2-pyridyl H O 189 Cl H CH₃ O 190 Cl CH₃ CH₃ O 191 Cl C₂H₅ CH₃ O 192 Cl n-C₃H₇ CH₃ O 193 Cl i-C₃H₇ CH₃ O 194 Cl n-C₄H₉ CH₃ O 195 Cl i-C₄H₉ CH₃ O 196 Cl s-C₄H₉ CH₃ O 197 Cl t-C₄H₉ CH₃ O 198 Cl CH₂OCH₃ CH₃ O 199 Cl CF₃ CH₃ O 200 Cl CF₂H CH₃ O 201 Cl CN CH₃ O 202 Cl OH CH₃ O 203 Cl OCH₃ CH₃ O 204 Cl NH₂ CH₃ O 205 Cl NHCH₃ CH₃ O 206 Cl N(CH₃)₂ CH₃ O 207 Cl CO₂CH₃ CH₃ O 208 Cl CO₂C₂H₅ CH₃ O 209 Cl C(O)CH₃ CH₃ O 210 Cl C(O)CF₃ CH₃ O 211 Cl C(═NOCH₃)CH₃ CH₃ O 212 Cl SO₂CH₃ CH₃ O 213 Cl SO₂CF₃ CH₃ O 214 Cl CH₂CO₂H CH₃ O 215 Cl CH₂COOCH₃ CH₃ O 216 Cl CH₂COOC₂H₅ CH₃ O 217 Cl prop-1-en-3-yl CH₃ O 218 Cl trans-but-2-en-1-yl CH₃ O 219 Cl cis-but-2-en-1-yl CH₃ O 220 Cl cis-3-methyl- CH₃ O but-2-en-1-yl 221 Cl cyclopropyl CH₃ O 222 Cl cyclopentyl CH₃ O 223 Cl cyclohexyl CH₃ O 224 Cl 4,5-dihydroisoxazol- CH₃ O 3-yl 225 Cl 4-methyl-4,5-dihydro- CH₃ O isoxazol-3-yl 226 Cl isoxazol-3-yl CH₃ O 227 Cl 4-methylisoxazol-3-yl CH₃ O 228 Cl 4,5-dihydroisoxazol- CH₃ O 4-yl 229 Cl 3-methyl-4,5-dihydro- CH₃ O isoxazol-4-yl 230 Cl isoxazol-4-yl CH₃ O 231 Cl 3-methylisoxazol-4-yl CH₃ O 232 Cl phenyl CH₃ O 233 Cl benzyl CH₃ O 234 Cl benzoyl CH₃ O 235 Cl 2-pyridyl CH₃ O 236 Cl H Cl O 237 Cl CH₃ Cl O 238 Cl C₂H₅ Cl O 239 Cl n-C₃H₇ Cl O 240 Cl i-C₃H₇ Cl O 241 Cl n-C₄H₉ Cl O 242 Cl i-C₄H₉ Cl O 243 Cl s-C₄H₉ Cl O 244 Cl t-C₄H₉ Cl O 245 Cl CH₂OCH₃ Cl O 246 Cl CF₃ Cl O 247 Cl CF₂H Cl O 248 Cl CN Cl O 249 Cl OH Cl O 250 Cl OCH₃ Cl O 251 Cl NH₂ Cl O 252 Cl NHCH₃ Cl O 253 Cl N(CH₃)₂ Cl O 254 Cl CO₂CH₃ Cl O 255 Cl CO₂C₂H₅ Cl O 256 Cl C(O)CH₃ Cl O 257 Cl C(O)CF₃ Cl O 258 Cl C(═NOCH₃)CH₃ Cl O 259 Cl SO₂CH₃ Cl O 260 Cl SO₂CF₃ Cl O 261 Cl CH₂CO₂H Cl O 262 Cl CH₂COOCH₃ Cl O 263 Cl CH₂COOC₂H₅ Cl O 264 Cl prop-1-en-3-yl Cl O 265 Cl trans-but-2-en-1-yl Cl O 266 Cl cis-but-2-en-1-yl Cl O 267 Cl cis-3-methyl- Cl O but-2-en-1-yl 268 Cl cyclopropyl Cl O 269 Cl cyclopentyl Cl O 270 Cl cyclohexyl Cl O 271 Cl 4,5-dihydroisoxazol- Cl O 3-yl 272 Cl 4-methyl-4,5-dihydro- Cl O isoxazol-3-yl 273 Cl isoxazol-3-yl Cl O 274 Cl 4-methylisoxazol-3-yl Cl O 275 Cl 4,5-dihydroisoxazol- Cl O 4-yl 276 Cl 3-methyl-4,5-dihydro- Cl O isoxazol-4-yl 277 Cl isoxazol-4-yl Cl O 278 Cl 3-methylisoxazol-4-yl Cl O 279 Cl phenyl Cl O 280 Cl benzyl Cl O 281 Cl benzoyl Cl O 282 Cl 2-pyridyl Cl O 283 OCH₃ H H O 284 OCH₃ CH₃ H O 285 OCH₃ C₂H₅ H O 286 OCH₃ n-C₃H₇ H O 287 OCH₃ i-C₃H₇ H O 288 OCH₃ n-C₄H₉ H O 289 OCH₃ i-C₄H₉ H O 290 OCH₃ s-C₄H₉ H O 291 OCH₃ t-C₄H₉ H O 292 OCH₃ CH₂OCH₃ H O 293 OCH₃ CF₃ H O 294 OCH₃ CF₂H H O 295 OCH₃ CN H O 296 OCH₃ OH H O 297 OCH₃ OCH₃ H O 298 OCH₃ NH₂ H O 299 OCH₃ NHCH₃ H O 300 OCH₃ N(CH₃)₂ H O 301 OCH₃ CO₂CH₃ H O 302 OCH₃ CO₂C₂H₅ H O 303 OCH₃ C(O)CH₃ H O 304 OCH₃ C(O)CF₃ H O 305 OCH₃ C(═NOCH₃)CH₃ H O 306 OCH₃ SO₂CH₃ H O 307 OCH₃ SO₂CF₃ H O 308 OCH₃ CH₂CO₂H H O 309 OCH₃ CH₂COOCH₃ H O 310 OCH₃ CH₂COOC₂H₅ H O 311 OCH₃ prop-1-en-3-yl H O 312 OCH₃ trans-but-2-en-1-yl H O 313 OCH₃ cis-but-2-en-1-yl H O 314 OCH₃ cis-3-methyl- H O but-2-en-1-yl 315 OCH₃ cyclopropyl H O 316 OCH₃ cyclopentyl H O 317 OCH₃ cyclohexyl H O 318 OCH₃ 4,5-dihydroisoxazol- H O 3-yl 319 OCH₃ 4-methyl-4,5-dihydro- H O isoxazol-3-yl 320 OCH₃ isoxazol-3-yl H O 321 OCH₃ 4-methylisoxazol-3-yl H O 322 OCH₃ 4,5-dihydroisoxazol- H O 4-yl 323 OCH₃ 3-methyl-4,5-dihydro- H O isoxazol-4-yl 324 OCH₃ isoxazol-4-yl H O 325 OCH₃ 3-methylisoxazol-4-yl H O 326 OCH₃ phenyl H O 327 OCH₃ benzyl H O 328 OCH₃ benzoyl H O 329 OCH₃ 2-pyridyl H O 330 OCH₃ H CH₃ O 331 OCH₃ CH₃ CH₃ O 332 OCH₃ C₂H₅ CH₃ O 333 OCH₃ n-C₃H₇ CH₃ O 334 OCH₃ i-C₃H₇ CH₃ O 335 OCH₃ n-C₄H₉ CH₃ O 336 OCH₃ i-C₄H₉ CH₃ O 337 OCH₃ s-C₄H₉ CH₃ O 338 OCH₃ t-C₄H₉ CH₃ O 339 OCH₃ CH₂OCH₃ CH₃ O 340 OCH₃ CF₃ CH₃ O 341 OCH₃ CF₂H CH₃ O 342 OCH₃ CN CH₃ O 343 OCH₃ OH CH₃ O 344 OCH₃ OCH₃ CH₃ O 345 OCH₃ NH₂ CH₃ O 346 OCH₃ NHCH₃ CH₃ O 347 OCH₃ N(CH₃)₂ CH₃ O 348 OCH₃ CO₂CH₃ CH₃ O 349 OCH₃ CO₂C₂H₅ CH₃ O 350 OCH₃ C(O)CH₃ CH₃ O 351 OCH₃ C(O)CF₃ CH₃ O 352 OCH₃ C(═NOCH₃)CH₃ CH₃ O 353 OCH₃ SO₂CH₃ CH₃ O 354 OCH₃ SO₂CF₃ CH₃ O 355 OCH₃ CH₂CO₂H CH₃ O 356 OCH₃ CH₂COOCH₃ CH₃ O 357 OCH₃ CH₂COOC₂H₅ CH₃ O 358 OCH₃ prop-1-en-3-yl CH₃ O 359 OCH₃ trans-but-2-en-1-yl CH₃ O 360 OCH₃ cis-but-2-en-1-yl CH₃ O 361 OCH₃ cis-3-methyl- CH₃ O but-2-en-1-yl 362 OCH₃ cyclopropyl CH₃ O 363 OCH₃ cyclopentyl CH₃ O 364 OCH₃ cyclohexyl CH₃ O 365 OCH₃ 4,5-dihydroisoxazol- CH₃ O 3-yl 366 OCH₃ 4-methyl-4,5-dihydro- CH₃ O isoxazol-3-yl 367 OCH₃ isoxazol-3-yl CH₃ O 368 OCH₃ 4-methylisoxazol-3-yl CH₃ O 369 OCH₃ 4,5-dihydroisoxazol- CH₃ O 4-yl 370 OCH₃ 3-methyl-4,5-dihydro- CH₃ O isoxazol-4-yl 371 OCH₃ isoxazol-4-yl CH₃ O 372 OCH₃ 3-methylisoxazol-4-yl CH₃ O 373 OCH₃ phenyl CH₃ O 374 OCH₃ benzyl CH₃ O 375 OCH₃ benzoyl CH₃ O 376 OCH₃ 2-pyridyl CH₃ O 377 OCH₃ H Cl O 378 OCH₃ CH₃ Cl O 379 OCH₃ C₂H₅ Cl O 380 OCH₃ n-C₃H₇ Cl O 381 OCH₃ i-C₃H₇ Cl O 382 OCH₃ n-C₄H₉ Cl O 383 OCH₃ i-C₄H₉ Cl O 384 OCH₃ s-C₄H₉ Cl O 385 OCH₃ t-C₄H₉ Cl O 386 OCH₃ CH₂OCH₃ Cl O 387 OCH₃ CF₃ Cl O 388 OCH₃ CF₂H Cl O 389 OCH₃ CN Cl O 390 OCH₃ OH Cl O 391 OCH₃ OCH₃ Cl O 392 OCH₃ NH₂ Cl O 393 OCH₃ NHCH₃ Cl O 394 OCH₃ N(CH₃)₂ Cl O 395 OCH₃ CO₂CH₃ Cl O 396 OCH₃ CO₂C₂H₅ Cl O 397 OCH₃ C(O)CH₃ Cl O 398 OCH₃ C(O)CF₃ Cl O 399 OCH₃ C(═NOCH₃)CH₃ Cl O 400 OCH₃ SO₂CH₃ Cl O 401 OCH₃ SO₂CF₃ Cl O 402 OCH₃ CH₂CO₂H Cl O 403 OCH₃ CH₂COOCH₃ Cl O 404 OCH₃ CH₂COOC₂H₅ Cl O 405 OCH₃ prop-1-en-3-yl Cl O 406 OCH₃ trans-but-2-en-1-yl Cl O 407 OCH₃ cis-but-2-en-1-yl Cl O 408 OCH₃ cis-3-methyl- Cl O but-2-en-1-yl 409 OCH₃ cyclopropyl Cl O 410 OCH₃ cyclopentyl Cl O 411 OCH₃ cyclohexyl Cl O 412 OCH₃ 4,5-dihydroisoxazol- Cl O 3-yl 413 OCH₃ 4-methyl-4,5-dihydro- Cl O isoxazol-3-yl 414 OCH₃ isoxazol-3-yl Cl O 415 OCH₃ 4-methylisoxazol-3-yl Cl O 416 OCH₃ 4,5-dihydroisoxazol- Cl O 4-yl 417 OCH₃ 3-methyl-4,5-dihydro- Cl O isoxazol-4-yl 418 OCH₃ isoxazol-4-yl Cl O 419 OCH₃ 3-methylisoxazol-4-yl Cl O 420 OCH₃ phenyl Cl O 421 OCH₃ benzyl Cl O 422 OCH₃ benzoyl Cl O 423 OCH₃ 2-pyridyl Cl O 424 OCF₃ H H O 425 OCF₃ CH₃ H O 426 OCF₃ C₂H₅ H O 427 OCF₃ n-C₃H₇ H O 428 OCF₃ i-C₃H₇ H O 429 OCF₃ n-C₄H₉ H O 430 OCF₃ i-C₄H₉ H O 431 OCF₃ s-C₄H₉ H O 432 OCF₃ t-C₄H₉ H O 433 OCF₃ CH₂OCH₃ H O 434 OCF₃ CF₃ H O 435 OCF₃ CF₂H H O 436 OCF₃ CN H O 437 OCF₃ OH H O 438 OCF₃ OCH₃ H O 439 OCF₃ NH₂ H O 440 OCF₃ NHCH₃ H O 441 OCF₃ N(CH₃)₂ H O 442 OCF₃ CO₂CH₃ H O 443 OCF₃ CO₂C₂H₅ H O 444 OCF₃ C(O)CH₃ H O 445 OCF₃ C(O)CF₃ H O 446 OCF₃ C(═NOCH₃)CH₃ H O 447 OCF₃ SO₂CH₃ H O 448 OCF₃ SO₂CF₃ H O 449 OCF₃ CH₂CO₂H H O 450 OCF₃ CH₂COOCH₃ H O 451 OCF₃ CH₂COOC₂H₅ H O 452 OCF₃ prop-1-en-3-yl H O 453 OCF₃ trans-but-2-en-1-yl H O 454 OCF₃ cis-but-2-en-1-yl H O 455 OCF₃ cis-3-methyl- H O but-2-en-1-yl 456 OCF₃ cyclopropyl H O 457 OCF₃ cyclopentyl H O 458 OCF₃ cyclohexyl H O 459 OCF₃ 4,5-dihydroisoxazol- H O 3-yl 460 OCF₃ 4-methyl-4,5-dihydro- H O isoxazol-3-yl 461 OCF₃ isoxazol-3-yl H O 462 OCF₃ 4-methylisoxazol-3-yl H O 463 OCF₃ 4,5-dihydroisoxazol- H O 4-yl 464 OCF₃ 3-methyl-4,5-dihydro- H O isoxazol-4-yl 465 OCF₃ isoxazol-4-yl H O 466 OCF₃ 3-methylisoxazol-4-yl H O 467 OCF₃ phenyl H O 468 OCF₃ benzyl H O 469 OCF₃ benzoyl H O 470 OCF₃ 2-pyridyl H O 471 OCF₃ H CH₃ O 472 OCF₃ CH₃ CH₃ O 473 OCF₃ C₂H₅ CH₃ O 474 OCF₃ n-C₃H₇ CH₃ O 475 OCF₃ i-C₃H₇ CH₃ O 476 OCF₃ n-C₄H₉ CH₃ O 477 OCF₃ i-C₄H₉ CH₃ O 478 OCF₃ s-C₄H₉ CH₃ O 479 OCF₃ t-C₄H₉ CH₃ O 480 OCF₃ CH₂OCH₃ CH₃ O 481 OCF₃ CF₃ CH₃ O 482 OCF₃ CF₂H CH₃ O 483 OCF₃ CN CH₃ O 484 OCF₃ OH CH₃ O 485 OCF₃ OCH₃ CH₃ O 486 OCF₃ NH₂ CH₃ O 487 OCF₃ NHCH₃ CH₃ O 488 OCF₃ N(CH₃)₂ CH₃ O 489 OCF₃ CO₂CH₃ CH₃ O 490 OCF₃ CO₂C₂H₅ CH₃ O 491 OCF₃ C(O)CH₃ CH₃ O 492 OCF₃ C(O)CF₃ CH₃ O 493 OCF₃ C(═NOCH₃)CH₃ CH₃ O 494 OCF₃ SO₂CH₃ CH₃ O 495 OCF₃ SO₂CF₃ CH₃ O 496 OCF₃ CH₂CO₂H CH₃ O 497 OCF₃ CH₂COOCH₃ CH₃ O 498 OCF₃ CH₂COOC₂H₅ CH₃ O 499 OCF₃ prop-1-en-3-yl CH₃ O 500 OCF₃ trans-but-2-en-1-yl CH₃ O 501 OCF₃ cis-but-2-en-1-yl CH₃ O 502 OCF₃ cis-3-methyl- CH₃ O but-2-en-1-yl 503 OCF₃ cyclopropyl CH₃ O 504 OCF₃ cyclopentyl CH₃ O 505 OCF₃ cyclohexyl CH₃ O 506 OCF₃ 4,5-dihydroisoxazol- CH₃ O 3-yl 507 OCF₃ 4-methyl-4,5-dihydro- CH₃ O isoxazol-3-yl 508 OCF₃ isoxazol-3-yl CH₃ O 509 OCF₃ 4-methylisoxazol-3-yl CH₃ O 510 OCF₃ 4,5-dihydroisoxazol- CH₃ O 4-yl 511 OCF₃ 3-methyl-4,5-dihydro- CH₃ O isoxazol-4-yl 512 OCF₃ isoxazol-4-yl CH₃ O 513 OCF₃ 3-methylisoxazol-4-yl CH₃ O 514 OCF₃ phenyl CH₃ O 515 OCF₃ benzyl CH₃ O 516 OCF₃ benzoyl CH₃ O 517 OCF₃ 2-pyridyl CH₃ O 518 OCF₃ H Cl O 519 OCF₃ CH₃ Cl O 520 OCF₃ C₂H₅ Cl O 521 OCF₃ n-C₃H₇ Cl O 522 OCF₃ i-C₃H₇ Cl O 523 OCF₃ n-C₄H₉ Cl O 524 OCF₃ i-C₄H₉ Cl O 525 OCF₃ s-C₄H₉ Cl O 526 OCF₃ t-C₄H₉ Cl O 527 OCF₃ CH₂OCH₃ Cl O 528 OCF₃ CF₃ Cl O 529 OCF₃ CF₂H Cl O 530 OCF₃ CN Cl O 531 OCF₃ OH Cl O 532 OCF₃ OCH₃ Cl O 533 OCF₃ NH₂ Cl O 534 OCF₃ NHCH₃ Cl O 535 OCF₃ N(CH₃)₂ Cl O 536 OCF₃ CO₂CH₃ Cl O 537 OCF₃ CO₂C₂H₅ Cl O 538 OCF₃ C(O)CH₃ Cl O 539 OCF₃ C(O)CF₃ Cl O 540 OCF₃ C(═NOCH₃)CH₃ Cl O 541 OCF₃ SO₂CH₃ Cl O 542 OCF₃ SO₂CF₃ Cl O 543 OCF₃ CH₂CO₂H Cl O 544 OCF₃ CH₂COOCH₃ Cl O 545 OCF₃ CH₂COOC₂H₅ Cl O 546 OCF₃ prop-1-en-3-yl Cl O 547 OCF₃ trans-but-2-en-1-yl Cl O 548 OCF₃ cis-but-2-en-1-yl Cl O 549 OCF₃ cis-3-methyl- Cl O but-2-en-1-yl 550 OCF₃ cyclopropyl Cl O 551 OCF₃ cyclopentyl Cl O 552 OCF₃ cyclohexyl Cl O 553 OCF₃ 4,5-dihydroisoxazol- Cl O 3-yl 554 OCF₃ 4-methyl-4,5-dihydro- Cl O isoxazol-3-yl 555 OCF₃ isoxazol-3-yl Cl O 556 OCF₃ 4-methylisoxazol-3-yl Cl O 557 OCF₃ 4,5-dihydroisoxazol- Cl O 4-yl 558 OCF₃ 3-methyl-4,5-dihydro- Cl O isoxazol-4-yl 559 OCF₃ isoxazol-4-yl Cl O 560 OCF₃ 3-methylisoxazol-4-yl Cl O 561 OCF₃ phenyl Cl O 562 OCF₃ benzyl Cl O 563 OCF₃ benzoyl Cl O 564 OCF₃ 2-pyridyl Cl O 565 SCH₃ H H O 566 SCH₃ CH₃ H O 567 SCH₃ C₂H₅ H O 568 SCH₃ n-C₃H₇ H O 569 SCH₃ i-C₃H₇ H O 570 SCH₃ n-C₄H₉ H O 571 SCH₃ i-C₄H₉ H O 572 SCH₃ s-C₄H₉ H O 573 SCH₃ t-C₄H₉ H O 574 SCH₃ CH₂OCH₃ H O 575 SCH₃ CF₃ H O 576 SCH₃ CF₂H H O 577 SCH₃ CN H O 578 SCH₃ OH H O 579 SCH₃ OCH₃ H O 580 SCH₃ NH₂ H O 581 SCH₃ NHCH₃ H O 582 SCH₃ N(CH₃)₂ H O 583 SCH₃ CO₂CH₃ H O 584 SCH₃ CO₂C₂H₅ H O 585 SCH₃ C(O)CH₃ H O 586 SCH₃ C(O)CF₃ H O 587 SCH₃ C(═NOCH₃)CH₃ H O 588 SCH₃ SO₂CH₃ H O 589 SCH₃ SO₂CF₃ H O 590 SCH₃ CH₂CO₂H H O 591 SCH₃ CH₂COOCH₃ H O 592 SCH₃ CH₂COOC₂H₅ H O 593 SCH₃ prop-1-en-3-yl H O 594 SCH₃ trans-but-2-en-1-yl H O 595 SCH₃ cis-but-2-en-1-yl H O 596 SCH₃ cis-3-methyl- H O but-2-en-1-yl 597 SCH₃ cyclopropyl H O 598 SCH₃ cyclopentyl H O 599 SCH₃ cyclohexyl H O 600 SCH₃ 4,5-dihydroisoxazol- H O 3-yl 601 SCH₃ 4-methyl-4,5-dihydro- H O isoxazol-3-yl 602 SCH₃ isoxazol-3-yl H O 603 SCH₃ 4-methylisoxazol-3-yl H O 604 SCH₃ 4,5-dihydroisoxazol- H O 4-yl O 605 SCH₃ 3-methyl-4,5-dihydro- H O isoxazol-4-yl H O 606 SCH₃ isoxazol-4-yl H O 607 SCH₃ 3-methylisoxazol-4-yl H O 608 SCH₃ phenyl H O 609 SCH₃ benzyl H O 610 SCH₃ benzoyl H O 611 SCH₃ 2-pyridyl H O 612 SCH₃ H CH₃ O 613 SCH₃ CH₃ CH₃ O 614 SCH₃ C₂H₅ CH₃ O 615 SCH₃ n-C₃H₇ CH₃ O 616 SCH₃ i-C₃H₇ CH₃ O 617 SCH₃ n-C₄H₉ CH₃ O 618 SCH₃ i-C₄H₉ CH₃ O 619 SCH₃ s-C₄H₉ CH₃ O 620 SCH₃ t-C₄H₉ CH₃ O 621 SCH₃ CH₂OCH₃ CH₃ O 622 SCH₃ CF₃ CH₃ O 623 SCH₃ CF₂H CH₃ O 624 SCH₃ CN CH₃ O 625 SCH₃ OH CH₃ O 626 SCH₃ OCH₃ CH₃ O 627 SCH₃ NH₂ CH₃ O 628 SCH₃ NHCH₃ CH₃ O 629 SCH₃ N(CH₃)₂ CH₃ O 630 SCH₃ CO₂CH₃ CH₃ O 631 SCH₃ CO₂C₂H₅ CH₃ O 632 SCH₃ C(O)CH₃ CH₃ O 633 SCH₃ C(O)CF₃ CH₃ O 634 SCH₃ C(═NOCH₃)CH₃ CH₃ O 635 SCH₃ SO₂CH₃ CH₃ O 636 SCH₃ SO₂CF₃ CH₃ O 637 SCH₃ CH₂CO₂H CH₃ O 638 SCH₃ CH₂COOCH₃ CH₃ O 639 SCH₃ CH₂COOC₂H₅ CH₃ O 640 SCH₃ prop-1-en-3-yl CH₃ O 641 SCH₃ trans-but-2-en-1-yl CH₃ O 642 SCH₃ cis-but-2-en-1-yl CH₃ O 643 SCH₃ cis-3-methyl- CH₃ O but-2-en-1-yl 644 SCH₃ cyclopropyl CH₃ O 645 SCH₃ cyclopentyl CH₃ O 646 SCH₃ cyclohexyl CH₃ O 647 SCH₃ 4,5-dihydroisoxazol- CH₃ O 3-yl 648 SCH₃ 4-methyl-4,5-dihydro- CH₃ O isoxazol-3-yl 649 SCH₃ isoxazol-3-yl CH₃ O 650 SCH₃ 4-methylisoxazol-3-yl CH₃ O 651 SCH₃ 4,5-dihydroisoxazol- CH₃ O 4-yl 652 SCH₃ 3-methyl-4,5-dihydro- CH₃ O isoxazol-4-yl 653 SCH₃ isoxazol-4-yl CH₃ O 654 SCH₃ 3-methylisoxazol-4-yl CH₃ O 655 SCH₃ phenyl CH₃ O 656 SCH₃ benzyl CH₃ O 657 SCH₃ benzoyl CH₃ O 658 SCH₃ 2-pyridyl CH₃ O 659 SCH₃ H Cl O 660 SCH₃ CH₃ Cl O 661 SCH₃ C₂H₅ Cl O 662 SCH₃ n-C₃H₇ Cl O 663 SCH₃ i-C₃H₇ Cl O 664 SCH₃ n-C₄H₉ Cl O 665 SCH₃ i-C₄H₉ Cl O 666 SCH₃ s-C₄H₉ Cl O 667 SCH₃ t-C₄H₉ Cl O 668 SCH₃ CH₂OCH₃ Cl O 669 SCH₃ CF₃ Cl O 670 SCH₃ CF₂H Cl O 671 SCH₃ CN Cl O 672 SCH₃ OH Cl O 673 SCH₃ OCH₃ Cl O 674 SCH₃ NH₂ Cl O 675 SCH₃ NHCH₃ Cl O 676 SCH₃ N(CH₃)₂ Cl O 677 SCH₃ CO₂CH₃ Cl O 678 SCH₃ CO₂C₂H₅ Cl O 679 SCH₃ C(O)CH₃ Cl O 680 SCH₃ C(O)CF₃ Cl O 681 SCH₃ C(═NOCH₃)CH₃ Cl O 682 SCH₃ SO₂CH₃ Cl O 683 SCH₃ SO₂CF₃ Cl O 684 SCH₃ CH₂CO₂H Cl O 685 SCH₃ CH₂COOCH₃ Cl O 686 SCH₃ CH₂COOC₂H₅ Cl O 687 SCH₃ prop-1-en-3-yl Cl O 688 SCH₃ trans-but-2-en-1-yl Cl O 689 SCH₃ cis-but-2-en-1-yl Cl O 690 SCH₃ cis-3-methyl- Cl O but-2-en-1-yl 691 SCH₃ cyclopropyl Cl O 692 SCH₃ cyclopentyl Cl O 693 SCH₃ cyclohexyl Cl O 694 SCH₃ 4,5-dihydroisoxazol- Cl O 3-yl 695 SCH₃ 4-methyl-4,5-dihydro- Cl O isoxazol-3-yl 696 SCH₃ isoxazol-3-yl Cl O 697 SCH₃ 4-methylisoxazol-3-yl Cl O 698 SCH₃ 4,5-dihydroisoxazol- Cl O 4-yl 699 SCH₃ 3-methyl-4,5-dihydro- Cl O isoxazol-4-yl 700 SCH₃ isoxazol-4-yl Cl O 701 SCH₃ 3-methylisoxazol-4-yl Cl O 702 SCH₃ phenyl Cl O 703 SCH₃ benzyl Cl O 704 SCH₃ benzoyl Cl O 705 SCH₃ 2-pyridyl Cl O 706 SO₂CH₃ H H O 707 SO₂CH₃ CH₃ H O 708 SO₂CH₃ C₂H₅ H O 709 SO₂CH₃ n-C₃H₇ H O 710 SO₂CH₃ i-C₃H₇ H O 711 SO₂CH₃ n-C₄H₉ H O 712 SO₂CH₃ i-C₄H₉ H O 713 SO₂CH₃ s-C₄H₉ H O 714 SO₂CH₃ t-C₄H₉ H O 715 SO₂CH₃ CH₂OCH₃ H O 716 SO₂CH₃ CF₃ H O 717 SO₂CH₃ CF₂H H O 718 SO₂CH₃ CN H O 719 SO₂CH₃ OH H O 720 SO₂CH₃ OCH₃ H O 721 SO₂CH₃ NH₂ H O 722 SO₂CH₃ NHCH₃ H O 723 SO₂CH₃ N(CH₃)₂ H O 724 SO₂CH₃ CO₂CH₃ H O 725 SO₂CH₃ CO₂C₂H₅ H O 726 SO₂CH₃ C(O)CH₃ H O 727 SO₂CH₃ C(O)CF₃ H O 728 SO₂CH₃ C(═NOCH₃)CH₃ H O 729 SO₂CH₃ SO₂CH₃ H O 730 SO₂CH₃ SO₂CF₃ H O 731 SO₂CH₃ CH₂CO₂H H O 732 SO₂CH₃ CH₂COOCH₃ H O 733 SO₂CH₃ CH₂COOC₂H₅ H O 734 SO₂CH₃ prop-1-en-3-yl H O 735 SO₂CH₃ trans-but-2-en-1-yl H O 736 SO₂CH₃ cis-but-2-en-1-yl H O 737 SO₂CH₃ cis-3-methyl- H O but-2-en-1-yl 738 SO₂CH₃ cyclopropyl H O 739 SO₂CH₃ cyclopentyl H O 740 SO₂CH₃ cyclohexyl H O 741 SO₂CH₃ 4,5-dihydroisoxazol- H O 3-yl 742 SO₂CH₃ 4-methyl-4,5-dihydro- H O isoxazol-3-yl 743 SO₂CH₃ isoxazol-3-yl H O 744 SO₂CH₃ 4-methylisoxazol-3-yl H O 745 SO₂CH₃ 4,5-dihydroisoxazol- H O 4-yl 746 SO₂CH₃ 3-methyl-4,5-dihydro- H O isoxazol-4-yl 747 SO₂CH₃ isoxazol-4-yl H O 748 SO₂CH₃ 3-methylisoxazol-4-yl H O 749 SO₂CH₃ phenyl H O 750 SO₂CH₃ benzyl H O 751 SO₂CH₃ benzoyl H O 752 SO₂CH₃ 2-pyridyl H O 753 SO₂CH₃ H CH₃ O 754 SO₂CH₃ CH₃ CH₃ O 755 SO₂CH₃ C₂H₅ CH₃ O 756 SO₂CH₃ n-C₃H₇ CH₃ O 757 SO₂CH₃ i-C₃H₇ CH₃ O 758 SO₂CH₃ n-C₄H₉ CH₃ O 759 SO₂CH₃ i-C₄H₉ CH₃ O 760 SO₂CH₃ s-C₄H₉ CH₃ O 761 SO₂CH₃ t-C₄H₉ CH₃ O 762 SO₂CH₃ CH₂OCH₃ CH₃ O 763 SO₂CH₃ CF₃ CH₃ O 764 SO₂CH₃ CF₂H CH₃ O 765 SO₂CH₃ CN CH₃ O 766 SO₂CH₃ OH CH₃ O 767 SO₂CH₃ OCH₃ CH₃ O 768 SO₂CH₃ NH₂ CH₃ O 769 SO₂CH₃ NHCH₃ CH₃ O 770 SO₂CH₃ N(CH₃)₂ CH₃ O 771 SO₂CH₃ CO₂CH₃ CH₃ O 772 SO₂CH₃ CO₂C₂H₅ CH₃ O 773 SO₂CH₃ C(O)CH₃ CH₃ O 774 SO₂CH₃ C(O)CF₃ CH₃ O 775 SO₂CH₃ C(═NOCH₃)CH₃ CH₃ O 776 SO₂CH₃ SO₂CH₃ CH₃ O 777 SO₂CH₃ SO₂CF₃ CH₃ O 778 SO₂CH₃ CH₂CO₂H CH₃ O 779 SO₂CH₃ CH₂COOCH₃ CH₃ O 780 SO₂CH₃ CH₂COOC₂H₅ CH₃ O 781 SO₂CH₃ prop-1-en-3-yl CH₃ O 782 SO₂CH₃ trans-but-2-en-1-yl CH₃ O 783 SO₂CH₃ cis-but-2-en-1-yl CH₃ O 784 SO₂CH₃ cis-3-methyl- CH₃ O but-2-en-1-yl 785 SO₂CH₃ cyclopropyl CH₃ O 786 SO₂CH₃ cyclopentyl CH₃ O 787 SO₂CH₃ cyclohexyl CH₃ O 788 SO₂CH₃ 4,5-dihydroisoxazol- CH₃ O 3-yl 789 SO₂CH₃ 4-methyl-4,5-dihydro- CH₃ O isoxazol-3-yl 790 SO₂CH₃ isoxazol-3-yl CH₃ O 791 SO₂CH₃ 4-methylisoxazol-3-yl CH₃ O 792 SO₂CH₃ 4,5-dihydroisoxazol- CH₃ O 4-yl 793 SO₂CH₃ 3-methyl-4,5-dihydro- CH₃ O isoxazol-4-yl 794 SO₂CH₃ isoxazol-4-yl CH₃ O 795 SO₂CH₃ 3-methylisoxazol-4-yl CH₃ O 796 SO₂CH₃ phenyl CH₃ O 797 SO₂CH₃ benzyl CH₃ O 798 SO₂CH₃ benzoyl CH₃ O 799 SO₂CH₃ 2-pyridyl CH₃ O 800 SO₂CH₃ H Cl O 801 SO₂CH₃ CH₃ Cl O 802 SO₂CH₃ C₂H₅ Cl O 803 SO₂CH₃ n-C₃H₇ Cl O 804 SO₂CH₃ i-C₃H₇ Cl O 805 SO₂CH₃ n-C₄H₉ Cl O 806 SO₂CH₃ i-C₄H₉ Cl O 807 SO₂CH₃ S-C₄H₉ Cl O 808 SO₂CH₃ t-C₄H₉ Cl O 809 SO₂CH₃ CH₂OCH₃ Cl O 810 SO₂CH₃ CF₃ Cl O 811 SO₂CH₃ CF₂H Cl O 812 SO₂CH₃ CN Cl O 813 SO₂CH₃ OH Cl O 814 SO₂CH₃ OCH₃ Cl O 815 SO₂CH₃ NH₂ Cl O 816 SO₂CH₃ NHCH₃ Cl O 817 SO₂CH₃ N(CH₃)₂ Cl O 818 SO₂CH₃ CO₂CH₃ Cl O 819 SO₂CH₃ CO₂C₂H₅ Cl O 820 SO₂CH₃ C(O)CH₃ Cl O 821 SO₂CH₃ C(O)CF₃ Cl O 822 SO₂CH₃ C(═NOCH₃)CH₃ Cl O 823 SO₂CH₃ SO₂CH₃ Cl O 824 SO₂CH₃ SO₂CF₃ Cl O 825 SO₂CH₃ CH₂CO₂H Cl O 826 SO₂CH₃ CH₂COOCH₃ Cl O 827 SO₂CH₃ CH₂COOC₂H₅ Cl O 828 SO₂CH₃ prop-1-en-3-yl Cl O 829 SO₂CH₃ trans-but-2-en-1-yl Cl O 830 SO₂CH₃ cis-but-2-en-1-yl Cl O 831 SO₂CH₃ cis-3-methyl- Cl O but-2-en-1-yl 832 SO₂CH₃ cyclopropyl Cl O 833 SO₂CH₃ cyclopentyl Cl O 834 SO₂CH₃ cyclohexyl Cl O 835 SO₂CH₃ 4,5-dihydroisoxazol- Cl O 3-yl 836 SO₂CH₃ 4-methyl-4,5-dihydro- Cl O isoxazol-3-yl 837 SO₂CH₃ isoxazol-3-yl Cl O 838 SO₂CH₃ 4-methylisoxazol-3-yl Cl O 839 SO₂CH₃ 4,5-dihydroisoxazol- Cl O 4-yl 840 SO₂CH₃ 3-methyl-4,5-dihydro- Cl O isoxazol-4-yl 841 SO₂CH₃ isoxazol-4-yl Cl O 842 SO₂CH₃ 3-methylisoxazol-4-yl Cl O 843 SO₂CH₃ phenyl Cl O 844 SO₂CH₃ benzyl Cl O 845 SO₂CH₃ benzoyl Cl O 846 SO₂CH₃ 2-pyridyl Cl O 847 CF₃ H H O 848 CF₃ CH₃ H O 849 CF₃ C₂H₅ H O 850 CF₃ n-C₃H₇ H O 851 CF₃ i-C₃H₇ H O 852 CF₃ n-C₄H₉ H O 853 CF₃ i-C₄H₉ H O 854 CF₃ s-C₄H₉ H O 855 CF₃ t-C₄H₉ H O 856 CF₃ CH₂OCH₃ H O 857 CF₃ CF₃ H O 858 CF₃ CF₂H H O 859 CF₃ CN H O 860 CF₃ OH H O 861 CF₃ OCH₃ H O 862 CF₃ NH₂ H O 863 CF₃ NHCH₃ H O 864 CF₃ N(CH₃)₂ H O 865 CF₃ CO₂CH₃ H O 866 CF₃ CO₂C₂H₅ H O 867 CF₃ C(O)CH₃ H O 868 CF₃ C(O)CF₃ H O 869 CF₃ C(═NOCH₃)CH₃ H O 870 CF₃ SO₂CH₃ H O 871 CF₃ SO₂CF₃ H O 872 CF₃ CH₂CO₂H H O 873 CF₃ CH₂COOCH₃ H O 874 CF₃ CH₂COOC₂H₅ H O 875 CF₃ prop-1-en-3-yl H O 876 CF₃ trans-but-2-en-1-yl H O 877 CF₃ cis-but-2-en-1-yl H O 878 CF₃ cis-3-methyl- H O but-2-en-1-yl 879 CF₃ cyclopropyl H O 880 CF₃ cyclopentyl H O 881 CF₃ cyclohexyl H O 882 CF₃ 4,5-dihydroisoxazol- H O 3-yl 883 CF₃ 4-methyl-4,5-dihydro- H O isoxazol-3-yl 884 CF₃ isoxazol-3-yl H O 885 CF₃ 4-methylisoxazol-3-yl H O 886 CF₃ 4,5-dihydroisoxazol- H O 4-yl 887 CF₃ 3-methyl-4,5-dihydro- H O isoxazol-4-yl 888 CF₃ isoxazol-4-yl H O 889 CF₃ 3-methylisoxazol-4-yl H O 890 CF₃ phenyl H O 891 CF₃ benzyl H O 892 CF₃ benzoyl H O 893 CF₃ 2-pyridyl H O 894 CF₃ H CH₃ O 895 CF₃ CH₃ CH₃ O 896 CF₃ C₂H₅ CH₃ O 897 CF₃ n-C₃H₇ CH₃ O 898 CF₃ i-C₃H₇ CH₃ O 899 CF₃ n-C₄H₉ CH₃ O 900 CF₃ i-C₄H₉ CH₃ O 901 CF₃ s-C₄H₉ CH₃ O 902 CF₃ t-C₄H₉ CH₃ O 903 CF₃ CH₂OCH₃ CH₃ O 904 CF₃ CF₃ CH₃ O 905 CF₃ CF₂H CH₃ O 906 CF₃ CN CH₃ O 907 CF₃ OH CH₃ O 908 CF₃ OCH₃ CH₃ O 909 CF₃ NH₂ CH₃ O 910 CF₃ NHCH₃ CH₃ O 911 CF₃ N(CH₃)₂ CH₃ O 912 CF₃ CO₂CH₃ CH₃ O 913 CF₃ CO₂C₂H₅ CH₃ O 914 CF₃ C(O)CH₃ CH₃ O 915 CF₃ C(O)CF₃ CH₃ O 916 CF₃ C(═NOCH₃)CH₃ CH₃ O 917 CF₃ SO₂CH₃ CH₃ O 918 CF₃ SO₂CF₃ CH₃ O 919 CF₃ CH₂CO₂H CH₃ O 920 CF₃ CH₂COOCH₃ CH₃ O 921 CF₃ CH₂COOC₂H₅ CH₃ O 922 CF₃ prop-1-en-3-yl CH₃ O 923 CF₃ trans-but-2-en-1-yl CH₃ O 924 CF₃ cis-but-2-en-1-yl CH₃ O 925 CF₃ cis-3-methyl- CH₃ O but-2-en-1-yl 926 CF₃ cyclopropyl CH₃ O 927 CF₃ cyclopentyl CH₃ O 928 CF₃ cyclohexyl CH₃ O 929 CF₃ 4,5-dihydroisoxazol- CH₃ O 3-yl 930 CF₃ 4-methyl-4,5-dihydroisoxazol- CH₃ O 3-yl 931 CF₃ isoxazol-3-yl CH₃ O 932 CF₃ 4-methylisoxazol-3-yl CH₃ O 933 CF₃ 4,5-dihydroisoxazol- CH₃ O 4-yl 934 CF₃ 3-methyl-4,5-dihydroisoxazol- CH₃ O 4-yl 935 CF₃ isoxazol-4-yl CH₃ O 936 CF₃ 3-methylisoxazol-4-yl CH₃ O 937 CF₃ phenyl CH₃ O 938 CF₃ benzyl CH₃ O 939 CF₃ benzoyl CH₃ O 940 CF₃ 2-pyridyl CH₃ O 941 CF₃ H Cl O 942 CF₃ CH₃ Cl O 943 CF₃ C₂H₅ Cl O 944 CF₃ n-C₃H₇ Cl O 945 CF₃ i-C₃H₇ Cl O 946 CF₃ n-C₄H₉ Cl O 947 CF₃ i-C₄H₉ Cl O 948 CF₃ s-C₄H₉ Cl O 949 CF₃ t-C₄H₉ Cl O 950 CF₃ CH₂OCH₃ Cl O 951 CF₃ CF₃ Cl O 952 CF₃ CF₂H Cl O 953 CF₃ CN Cl O 954 CF₃ OH Cl O 955 CF₃ OCH₃ Cl O 956 CF₃ NH₂ Cl O 957 CF₃ NHCH₃ Cl O 958 CF₃ N(CH₃)₂ Cl O 959 CF₃ CO₂CH₃ Cl O 960 CF₃ CO₂C₂H₅ Cl O 961 CF₃ C(O)CH₃ Cl O 962 CF₃ C(O)CF₃ Cl O 963 CF₃ C(═NOCH₃)CH₃ Cl O 964 CF₃ SO₂CH₃ Cl O 965 CF₃ SO₂CF₃ Cl O 966 CF₃ CH₂CO₂H Cl O 967 CF₃ CH₂COOCH₃ Cl O 968 CF₃ CH₂COOC₂H₅ Cl O 969 CF₃ prop-1-en-3-yl Cl O 970 CF₃ trans-but-2-en-1-yl Cl O 971 CF₃ cis-but-2-en-1-yl Cl O 972 CF₃ cis-3-methyl- Cl O but-2-en-1-yl 973 CF₃ cyclopropyl Cl O 974 CF₃ cyclopentyl Cl O 975 CF₃ cyclohexyl Cl O 976 CF₃ 4,5-dihydroisoxazol- Cl O 3-yl 977 CF₃ 4-methyl-4,5-dihydroisoxazol- Cl O 3-yl 978 CF₃ isoxazol-3-yl Cl O 979 CF₃ 4-methylisoxazol-3-yl Cl O 980 CF₃ 4,5-dihydroisoxazol- Cl O 4-yl 981 CF₃ 3-methyl-4,5-dihydroisoxazol- Cl O 4-yl 982 CF₃ isoxazol-4-yl Cl O 983 CF₃ 3-methylisoxazol-4-yl Cl O 984 CF₃ phenyl Cl O 985 CF₃ benzyl Cl O 986 CF₃ benzoyl Cl O 987 CF₃ 2-pyridyl Cl O 988 C₂H₅ H H O 989 C₂H₅ CH₃ H O 990 C₂H₅ C₂H₅ H O 991 C₂H₅ n-C₃H₇ H O 992 C₂H₅ i-C₃H₇ H O 993 C₂H₅ n-C₄H₉ H O 994 C₂H₅ i-C₄H₉ H O 995 C₂H₅ s-C₄H₉ H O 996 C₂H₅ t-C₄H₉ H O 997 C₂H₅ CH₂OCH₃ H O 998 C₂H₅ CF₃ H O 999 C₂H₅ CF₂H H O 1000 C₂H₅ CN H O 1001 C₂H₅ OH H O 1002 C₂H₅ OCH₃ H O 1003 C₂H₅ NH₂ H O 1004 C₂H₅ NHCH₃ H O 1005 C₂H₅ N(CH₃)₂ H O 1006 C₂H₅ CO₂CH₃ H O 1007 C₂H₅ CO₂C₂H₅ H O 1008 C₂H₅ C(O)CH₃ H O 1009 C₂H₅ C(O)CF₃ H O 1010 C₂H₅ C(═NOCH₃)CH₃ H O 1011 C₂H₅ SO₂CH₃ H O 1012 C₂H₅ SO₂CF₃ H O 1013 C₂H₅ CH₂CO₂H H O 1014 C₂H₅ CH₂COOCH₃ H O 1015 C₂H₅ CH₂COOC₂H₅ H O 1016 C₂H₅ prop-1-en-3-yl H O 1017 C₂H₅ trans-but-2-en-1-yl H O 1018 C₂H₅ cis-but-2-en-1-yl H O 1019 C₂H₅ cis-3-methyl- H O but-2-en-1-yl 1020 C₂H₅ cyclopropyl H O 1021 C₂H₅ cyclopentyl H O 1022 C₂H₅ cyclohexyl H O 1023 C₂H₅ 4,5-dihydroisoxazol- H O 3-yl 1024 C₂H₅ 4-methyl-4,5-dihydroisoxazol- H O 3-yl 1025 C₂H₅ isoxazol-3-yl H O 1026 C₂H₅ 4-methylisoxazol-3-yl H O 1027 C₂H₅ 4,5-dihydroisoxazol- H O 4-yl 1028 C₂H₅ 3-methyl-4,5-dihydroisoxazol- H O 4-yl 1029 C₂H₅ isoxazol-4-yl H O 1030 C₂H₅ 3-methylisoxazol-4-yl H O 1031 C₂H₅ phenyl H O 1032 C₂H₅ benzyl H O 1033 C₂H₅ benzoyl H O 1034 C₂H₅ 2-pyridyl H O 1035 C₂H₅ H CH₃ O 1036 C₂H₅ CH₃ CH₃ O 1037 C₂H₅ C₂H₅ CH₃ O 1038 C₂H₅ n-C₃H₇ CH₃ O 1039 C₂H₅ i-C₃H₇ CH₃ O 1040 C₂H₅ n-C₄H₉ CH₃ O 1041 C₂H₅ i-C₄H₉ CH₃ O 1042 C₂H₅ s-C₄H₉ CH₃ O 1043 C₂H₅ t-C₄H₉ CH₃ O 1044 C₂H₅ CH₂OCH₃ CH₃ O 1045 C₂H₅ CF₃ CH₃ O 1046 C₂H₅ CF₂H CH₃ O 1047 C₂H₅ CN CH₃ O 1048 C₂H₅ OH CH₃ O 1049 C₂H₅ OCH₃ CH₃ O 1050 C₂H₅ NH₂ CH₃ O 1051 C₂H₅ NHCH₃ CH₃ O 1052 C₂H₅ N(CH₃)₂ CH₃ O 1053 C₂H₅ CO₂CH₃ CH₃ O 1054 C₂H₅ CO₂C₂H₅ CH₃ O 1055 C₂H₅ C(O)CH₃ CH₃ O 1056 C₂H₅ C(O)CF₃ CH₃ O 1057 C₂H₅ C(═NOCH₃)CH₃ CH₃ O 1058 C₂H₅ SO₂CH₃ CH₃ O 1059 C₂H₅ SO₂CF₃ CH₃ O 1060 C₂H₅ CH₂CO₂H CH₃ O 1061 C₂H₅ CH₂COOCH₃ CH₃ O 1062 C₂H₅ CH₂COOC₂H₅ CH₃ O 1063 C₂H₅ prop-1-en-3-yl CH₃ O 1064 C₂H₅ trans-but-2-en-1-yl CH₃ O 1065 C₂H₅ cis-but-2-en-1-yl CH₃ O 1066 C₂H₅ cis-3-methyl- CH₃ O but-2-en-1-yl 1067 C₂H₅ cyclopropyl CH₃ O 1068 C₂H₅ cyclopentyl CH₃ O 1069 C₂H₅ cyclohexyl CH₃ O 1070 C₂H₅ 4,5-dihydroisoxazol- CH₃ O 3-yl 1071 C₂H₅ 4-methyl-4,5-dihydroisoxazol- CH₃ O 3-yl 1072 C₂H₅ isoxazol-3-yl CH₃ O 1073 C₂H₅ 4-methylisoxazol-3-yl CH₃ O 1074 C₂H₅ 4,5-dihydroisoxazol- CH₃ O 4-yl 1075 C₂H₅ 3-methyl-4,5-dihydroisoxazol- CH₃ O 4-yl 1076 C₂H₅ isoxazol-4-yl CH₃ O 1077 C₂H₅ 3-methylisoxazol-4-yl CH₃ O 1078 C₂H₅ phenyl CH₃ O 1079 C₂H₅ benzyl CH₃ O 1080 C₂H₅ benzoyl CH₃ O 1081 C₂H₅ 2-pyridyl CH₃ O 1082 C₂H₅ H Cl O 1083 C₂H₅ CH₃ Cl O 1084 C₂H₅ C₂H₅ Cl O 1085 C₂H₅ n-C₃H₇ Cl O 1086 C₂H₅ i-C₃H₇ Cl O 1087 C₂H₅ n-C₄H₉ Cl O 1088 C₂H₅ i-C₄H₉ Cl O 1089 C₂H₅ s-C₄H₉ Cl O 1090 C₂H₅ t-C₄H₉ Cl O 1091 C₂H₅ CH₂OCH₃ Cl O 1092 C₂H₅ CF₃ Cl O 1093 C₂H₅ CF₂H Cl O 1094 C₂H₅ CN Cl O 1095 C₂H₅ OH Cl O 1096 C₂H₅ OCH₃ Cl O 1097 C₂H₅ NH₂ Cl O 1098 C₂H₅ NHCH₃ Cl O 1099 C₂H₅ N(CH₃)₂ Cl O 1100 C₂H₅ CO₂CH₃ Cl O 1101 C₂H₅ CO₂C₂H₅ Cl O 1102 C₂H₅ C(O)CH₃ Cl O 1103 C₂H₅ C(O)CF₃ Cl O 1104 C₂H₅ C(═NOCH₃)CH₃ Cl O 1105 C₂H₅ SO₂CH₃ Cl O 1106 C₂H₅ SO₂CF₃ Cl O 1107 C₂H₅ CH₂CO₂H Cl O 1108 C₂H₅ CH₂COOCH₃ Cl O 1109 C₂H₅ CH₂COOC₂H₅ Cl O 1110 C₂H₅ prop-1-en-3-yl Cl O 1111 C₂H₅ trans-but-2-en-1-yl Cl O 1112 C₂H₅ cis-but-2-en-1-yl Cl O 1113 C₂H₅ cis-3-methyl- Cl O but-2-en-1-yl 1114 C₂H₅ cyclopropyl Cl O 1115 C₂H₅ cyclopentyl Cl O 1116 C₂H₅ cyclohexyl Cl O 1117 C₂H₅ 4,5-dihydroisoxazol- Cl O 3-yl 1118 C₂H₅ 4-methyl-4,5-dihydroisoxazol- Cl O 3-yl 1119 C₂H₅ isoxazol-3-yl Cl O 1120 C₂H₅ 4-methylisoxazol-3-yl Cl O 1121 C₂H₅ 4,5-dihydroisoxazol- Cl O 4-yl 1122 C₂H₅ 3-methyl-4,5-dihydroisoxazol- Cl O 4-yl 1123 C₂H₅ isoxazol-4-yl Cl O 1124 C₂H₅ 3-methylisoxazol-4-yl Cl O 1125 C₂H₅ phenyl Cl O 1126 C₂H₅ benzyl Cl O 1127 C₂H₅ benzoyl Cl O 1128 C₂H₅ 2-pyridyl Cl O 1129 CH₃ CH₃ H S 1130 CH₃ H H S 1131 CH₃ C₂H₅ H S 1132 CH₃ n-C₃H₇ H S 1133 CH₃ i-C₃H₇ H S 1134 CH₃ n-C₄H₉ H S 1135 CH₃ i-C₄H₉ H S 1136 CH₃ s-C₄H₉ H S 1137 CH₃ t-C₄H₉ H S 1138 CH₃ CH₂OCH₃ H S 1139 CH₃ CF₃ H S 1140 CH₃ CF₂H H S 1141 CH₃ CN H S 1142 CH₃ OH H S 1143 CH₃ OCH₃ H S 1144 CH₃ NH₂ H S 1145 CH₃ NHCH₃ H S 1146 CH₃ N(CH₃)₂ H S 1147 CH₃ CO₂CH₃ H S 1148 CH₃ CO₂C₂H₅ H S 1149 CH₃ C(O)CH₃ H S 1150 CH₃ C(O)CF₃ H S 1151 CH₃ C(═NOCH₃)CH₃ H S 1152 CH₃ SO₂CH₃ H S 1153 CH₃ SO₂CF₃ H S 1154 CH₃ CH₂CO₂H H S 1155 CH₃ CH₂COOCH₃ H S 1156 CH₃ CH₂COOC₂H₅ H S 1157 CH₃ prop-1-en-3-yl H S 1158 CH₃ trans-but-2-en-1-yl H S 1159 CH₃ cis-but-2-en-1-yl H S 1160 CH₃ cis-3-methyl- H S but-2-en-1-yl 1161 CH₃ cyclopropyl H S 1162 CH₃ cyclopentyl H S 1163 CH₃ cyclohexyl H S 1164 CH₃ 4,5-dihydroisoxazol- H S 3-yl 1165 CH₃ 4-methyl-4,5-dihydro- H S isoxazol-3-yl 1166 CH₃ isoxazol-3-yl H S 1167 CH₃ 4-methylisoxazol-3-yl H S 1168 CH₃ 4,5-dihydroisoxazol- H S 4-yl 1169 CH₃ 3-methyl-4,5-dihydro- H S isoxazol-4-yl 1170 CH₃ isoxazol-4-yl H S 1171 CH₃ 3-methylisoxazol-4-yl H S 1172 CH₃ phenyl H S 1173 CH₃ benzyl H S 1174 CH₃ benzoyl H S 1175 CH₃ 2-pyridyl H S 1176 CH₃ H CH₃ S 1177 CH₃ CH₃ CH₃ S 1178 CH₃ C₂H₅ CH₃ S 1179 CH₃ n-C₃H₇ CH₃ S 1180 CH₃ i-C₃H₇ CH₃ S 1181 CH₃ n-C₄H₉ CH₃ S 1182 CH₃ i-C₄H₉ CH₃ S 1183 CH₃ s-C₄H₉ CH₃ S 1184 CH₃ t-C₄H₉ CH₃ S 1185 CH₃ CH₂OCH₃ CH₃ S 1186 CH₃ CF₃ CH₃ S 1187 CH₃ CF₂H CH₃ S 1188 CH₃ CN CH₃ S 1189 CH₃ OH CH₃ S 1190 CH₃ OCH₃ CH₃ S 1191 CH₃ NH₂ CH₃ S 1192 CH₃ NHCH₃ CH₃ S 1193 CH₃ N(CH₃)₂ CH₃ S 1194 CH₃ CO₂CH₃ CH₃ S 1195 CH₃ CO₂C₂H₅ CH₃ S 1196 CH₃ C(O)CH₃ CH₃ S 1197 CH₃ C(O)CF₃ CH₃ S 1198 CH₃ C(═NOCH₃)CH₃ CH₃ S 1199 CH₃ SO₂CH₃ CH₃ S 1200 CH₃ SO₂CF₃ CH₃ S 1201 CH₃ CH₂CO₂H CH₃ S 1202 CH₃ CH₂COOCH₃ CH₃ S 1203 CH₃ CH₂COOC₂H₅ CH₃ S 1204 CH₃ prop-1-en-3-yl CH₃ S 1205 CH₃ trans-but-2-en-1-yl CH₃ S 1206 CH₃ cis-but-2-en-1-yl CH₃ S 1207 CH₃ cis-3-methyl- CH₃ S but-2-en-1-yl 1208 CH₃ cyclopropyl CH₃ S 1209 CH₃ cyclopentyl CH₃ S 1210 CH₃ cyclohexyl CH₃ S 1211 CH₃ 4,5-dihydroisoxazol- CH₃ S 3-yl 1212 CH₃ 4-methyl-4,5-dihydro- CH₃ S isoxazol-3-yl 1213 CH₃ isoxazol-3-yl CH₃ S 1214 CH₃ 4-methylisoxazol-3-yl CH₃ S 1215 CH₃ 4,5-dihydroisoxazol- CH₃ S 4-yl 1216 CH₃ 3-methyl-4,5-dihydro- CH₃ S isoxazol-4-yl 1217 CH₃ isoxazol-4-yl CH₃ S 1218 CH₃ 3-methylisoxazol-4-yl CH₃ S 1219 CH₃ phenyl CH₃ S 1220 CH₃ benzyl CH₃ S 1221 CH₃ benzoyl CH₃ S 1222 CH₃ 2-pyridyl CH₃ S 1223 CH₃ H Cl S 1224 CH₃ CH₃ Cl S 1225 CH₃ C₂H₅ Cl S 1226 CH₃ n-C₃H₇ Cl S 1227 CH₃ i-C₃H₇ Cl S 1228 CH₃ n-C₄H₉ Cl S 1229 CH₃ i-C₄H₉ Cl S 1230 CH₃ s-C₄H₉ Cl S 1231 CH₃ t-C₄H₉ Cl S 1232 CH₃ CH₂OCH₃ Cl S 1233 CH₃ CF₃ Cl S 1234 CH₃ CF₂H Cl S 1235 CH₃ CN Cl S 1236 CH₃ OH Cl S 1237 CH₃ OCH₃ Cl S 1238 CH₃ NH₂ Cl S 1239 CH₃ NHCH₃ Cl S 1240 CH₃ N(CH₃)₂ Cl S 1241 CH₃ CO₂CH₃ Cl S 1242 CH₃ CO₂C₂H₅ Cl S 1243 CH₃ C(O)CH₃ Cl S 1244 CH₃ C(O)CF₃ Cl S 1245 CH₃ C(═NOCH₃)CH₃ Cl S 1246 CH₃ SO₂CH₃ Cl S 1247 CH₃ SO₂CF₃ Cl S 1248 CH₃ CH₂CO₂H Cl S 1249 CH₃ CH₂COOCH₃ Cl S 1250 CH₃ CH₂COOC₂H₅ Cl S 1251 CH₃ prop-1-en-3-yl Cl S 1252 CH₃ trans-but-2-en-1-yl Cl S 1253 CH₃ cis-but-2-en-1-yl Cl S 1254 CH₃ cis-3-methyl- Cl S but-2-en-1-yl 1255 CH₃ cyclopropyl Cl S 1256 CH₃ cyclopentyl Cl S 1257 CH₃ cyclohexyl Cl S 1258 CH₃ 4,5-dihydroisoxazol- Cl S 3-yl 1259 CH₃ 4-methyl-4,5-dihydro- Cl S isoxazol-3-yl 1260 CH₃ isoxazol-3-yl Cl S 1261 CH₃ 4-methylisoxazol-3-yl Cl S 1262 CH₃ 4,5-dihydroisoxazol- Cl S 4-yl 1263 CH₃ 3-methyl-4,5-dihydro- Cl S isoxazol-4-yl 1264 CH₃ isoxazol-4-yl Cl S 1265 CH₃ 3-methylisoxazol-4-yl Cl S 1266 CH₃ phenyl Cl S 1267 CH₃ benzyl Cl S 1268 CH₃ benzoyl Cl S 1269 CH₃ 2-pyridyl Cl S 1270 Cl H H S 1271 Cl CH₃ H S 1272 Cl C₂H₅ H S 1273 Cl n-C₃H₇ H S 1274 Cl i-C₃H₇ H S 1275 Cl n-C₄H₉ H S 1276 Cl i-C₄H₉ H S 1277 Cl s-C₄H₉ H S 1278 Cl t-C₄H₉ H S 1279 Cl CH₂OCH₃ H S 1280 Cl CF₃ H S 1281 Cl CF₂H H S 1282 Cl CN H S 1283 Cl OH H S 1284 Cl OCH₃ H S 1285 Cl NH₂ H S 1286 Cl NHCH₃ H S 1287 Cl N(CH₃)₂ H S 1288 Cl CO₂CH₃ H S 1289 Cl CO₂C₂H₅ H S 1290 Cl C(O)CH₃ H S 1291 Cl C(O)CF₃ H S 1292 Cl C(═NOCH₃)CH₃ H S 1293 Cl SO₂CH₃ H S 1294 Cl SO₂CF₃ H S 1295 Cl CH₂CO₂H H S 1296 Cl CH₂COOCH₃ H S 1297 Cl CH₂COOC₂H₅ H S 1298 Cl Prop-1-en-3-yl H S 1299 Cl trans-but-2-en-1-yl H S 1300 Cl cis-but-2-en-1-yl H S 1301 Cl cis-3-methyl- H S but-2-en-1-yl 1302 Cl cyclopropyl H S 1303 Cl cyclopentyl H S 1304 Cl cyclohexyl H S 1305 Cl 4,5-dihydroisoxazol- H S 3-yl 1306 Cl 4-methyl-4,5-dihydro- H S isoxazol-3-yl 1307 Cl isoxazol-3-yl H S 1308 Cl 4-methylisoxazol-3-yl H S 1309 Cl 4,5-dihydroisoxazol- H S 4-yl 1310 Cl 3-methyl-4,5-dihydro- H S isoxazol-4-yl 1311 Cl isoxazol-4-yl H S 1312 Cl 3-methylisoxazol-4-yl H S 1313 Cl phenyl H S 1314 Cl benzyl H S 1315 Cl benzoyl H S 1316 Cl 2-pyridyl H S 1317 Cl H CH₃ S 1318 Cl CH₃ CH₃ S 1319 Cl C₂H₅ CH₃ S 1320 Cl n-C₃H₇ CH₃ S 1321 Cl i-C₃H₇ CH₃ S 1322 Cl n-C₄H₉ CH₃ S 1323 Cl i-C₄H₉ CH₃ S 1324 Cl s-C₄H₉ CH₃ S 1325 Cl t-C₄H₉ CH₃ S 1326 Cl CH₂OCH₃ CH₃ S 1327 Cl CF₃ CH₃ S 1328 Cl CF₂H CH₃ S 1329 Cl CN CH₃ S 1330 Cl OH CH₃ S 1331 Cl OCH₃ CH₃ S 1332 Cl NH₂ CH₃ S 1333 Cl NHCH₃ CH₃ S 1334 Cl N(CH₃)₂ CH₃ S 1335 Cl CO₂CH₃ CH₃ S 1336 Cl CO₂C₂H₅ CH₃ S 1337 Cl C(O)CH₃ CH₃ S 1338 Cl C(O)CF₃ CH₃ S 1339 Cl C(═NOCH₃)CH₃ CH₃ S 1340 Cl SO₂CH₃ CH₃ S 1341 Cl SO₂CF₃ CH₃ S 1342 Cl CH₂CO₂H CH₃ S 1343 Cl CH₂COOCH₃ CH₃ S 1344 Cl CH₂COOC₂H₅ CH₃ S 1345 Cl prop-1-en-3-yl CH₃ S 1346 Cl trans-but-2-en-1-yl CH₃ S 1347 Cl cis-but-2-en-1-yl CH₃ S 1348 Cl cis-3-methyl- CH₃ S but-2-en-1-yl 1349 Cl cyclopropyl CH₃ S 1350 Cl cyclopentyl CH₃ S 1351 Cl cyclohexyl CH₃ S 1352 Cl 4,5-dihydroisoxazol- CH₃ S 3-yl 1353 Cl 4-methyl-4,5-dihydro- CH₃ S isoxazol-3-yl 1354 Cl isoxazol-3-yl CH₃ S 1355 Cl 4-methylisoxazol-3-yl CH₃ S 1356 Cl 4,5-dihydroisoxazol- CH₃ S 4-yl 1357 Cl 3-methyl-4,5-dihydro- CH₃ S isoxazol-4-yl 1358 Cl isoxazol-4-yl CH₃ S 1359 Cl 3-methylisoxazol-4-yl CH₃ S 1360 Cl phenyl CH₃ S 1361 Cl benzyl CH₃ S 1362 Cl benzoyl CH₃ S 1363 Cl 2-pyridyl CH₃ S 1364 Cl H Cl S 1365 Cl CH₃ Cl S 1366 Cl C₂H₅ Cl S 1367 Cl n-C₃H₇ Cl S 1368 Cl i-C₃H₇ Cl S 1369 Cl n-C₄H₉ Cl S 1370 Cl i-C₄H₉ Cl S 1371 Cl s-C₄H₉ Cl S 1372 Cl t-C₄H₉ Cl S 1373 Cl CH₂OCH₃ Cl S 1374 Cl CF₃ Cl S 1375 Cl CF₂H Cl S 1376 Cl CN Cl S 1377 Cl OH Cl S 1378 Cl OCH₃ Cl S 1379 Cl NH₂ Cl S 1380 Cl NHCH₃ Cl S 1381 Cl N(CH₃)₂ Cl S 1382 Cl CO₂CH₃ Cl S 1383 Cl CO₂C₂H₅ Cl S 1384 Cl C(O)CH₃ Cl S 1385 Cl C(O)CF₃ Cl S 1386 Cl C(═NOCH₃)CH₃ Cl S 1387 Cl SO₂CH₃ Cl S 1388 Cl SO₂CF₃ Cl S 1389 Cl CH₂CO₂H Cl S 1390 Cl CH₂COOCH₃ Cl S 1391 Cl CH₂COOC₂H₅ Cl S 1392 Cl prop-1-en-3-yl Cl S 1393 Cl trans-but-2-en-1-yl Cl S 1394 Cl cis-but-2-en-1-yl Cl S 1395 Cl cis-3-methyl- Cl S but-2-en-1-yl 1396 Cl cyclopropyl Cl S 1397 Cl cyclopentyl Cl S 1398 Cl cyclohexyl Cl S 1399 Cl 4,5-dihydroisoxazol- Cl S 3-yl 1400 Cl 4-methyl-4,5-dihydro- Cl S isoxazol-3-yl 1401 Cl isoxazol-3-yl Cl S 1402 Cl 4-methylisoxazol-3-yl Cl S 1403 Cl 4,5-dihydroisoxazol- Cl S 4-yl 1404 Cl 3-methyl-4,5-dihydro- Cl S isoxazol-4-yl 1405 Cl isoxazol-4-yl Cl S 1406 Cl 3-methylisoxazol-4-yl Cl S 1407 Cl phenyl Cl S 1408 Cl benzyl Cl S 1409 Cl benzoyl Cl S 1410 Cl 2-pyridyl Cl s 1411 OCH₃ H H S 1412 OCH₃ CH₃ H S 1413 OCH₃ C₂H₅ H S 1414 OCH₃ n-C₃H₇ H S 1415 OCH₃ i-C₃H₇ H S 1416 OCH₃ n-C₄H₉ H S 1417 OCH₃ i-C₄H₉ H S 1418 OCH₃ s-C₄H₉ H S 1419 OCH₃ t-C₄H₉ H S 1420 OCH₃ CH₂OCH₃ H S 1421 OCH₃ CF₃ H S 1422 OCH₃ CF₂H H S 1423 OCH₃ CN H S 1424 OCH₃ OH H S 1425 OCH₃ OCH₃ H S 1426 OCH₃ NH₂ H S 1427 OCH₃ NHCH₃ H S 1428 OCH₃ N(CH₃)₂ H S 1429 OCH₃ CO₂CH₃ H S 1430 OCH₃ CO₂C₂H₅ H S 1431 OCH₃ C(O)CH₃ H S 1432 OCH₃ C(O)CF₃ H S 1433 OCH₃ C(═NOCH₃)CH₃ H S 1434 OCH₃ SO₂CH₃ H S 1435 OCH₃ SO₂CF₃ H S 1436 OCH₃ CH₂CO₂H H S 1437 OCH₃ CH₂COOCH₃ H S 1438 OCH₃ CH₂COOC₂H₅ H S 1439 OCH₃ prop-1-en-3-yl H S 1440 OCH₃ trans-but-2-en-1-yl H S 1441 OCH₃ cis-but-2-en-1-yl H S 1442 OCH₃ cis-3-methyl- H S but-2-en-1-yl 1443 OCH₃ cyclopropyl H S 1444 OCH₃ cyclopentyl H S 1445 OCH₃ cyclohexyl H S 1446 OCH₃ 4,5-dihydroisoxazol- H S 3-yl 1447 OCH₃ 4-methyl-4,5-dihydro- H S isoxazol-3-yl 1448 OCH₃ isoxazol-3-yl H S 1449 OCH₃ 4-methylisoxazol-3-yl H S 1450 OCH₃ 4,5-dihydroisoxazol- H S 4-yl 1451 OCH₃ 3-methyl-4,5-dihydro- H S isoxazol-4-yl 1452 OCH₃ isoxazol-4-yl H S 1453 OCH₃ 3-methylisoxazol-4-yl H S 1454 OCH₃ phenyl H S 1455 OCH₃ benzyl H S 1456 OCH₃ benzoyl H S 1457 OCH₃ 2-pyridyl H S 1458 OCH₃ H CH₃ S 1459 OCH₃ CH₃ CH₃ S 1460 OCH₃ C₂H₅ CH₃ S 1461 OCH₃ n-C₃H₇ CH₃ S 1462 OCH₃ i-C₃H₇ CH₃ S 1463 OCH₃ n-C₄H₉ CH₃ S 1464 OCH₃ i-C₄H₉ CH₃ S 1465 OCH₃ s-C₄H₉ CH₃ S 1466 OCH₃ t-C₄H₉ CH₃ S 1467 OCH₃ CH₂OCH₃ CH₃ S 1468 OCH₃ CF₃ CH₃ S 1469 OCH₃ CF₂H CH₃ S 1470 OCH₃ CN CH₃ S 1471 OCH₃ OH CH₃ S 1472 OCH₃ OCH₃ CH₃ S 1473 OCH₃ NH₂ CH₃ S 1474 OCH₃ NHCH₃ CH₃ S 1475 OCH₃ N(CH₃)₂ CH₃ S 1476 OCH₃ CO₂CH₃ CH₃ S 1477 OCH₃ CO₂C₂H₅ CH₃ S 1478 OCH₃ C(O)CH₃ CH₃ S 1479 OCH₃ C(O)CF₃ CH₃ S 1480 OCH₃ C(═NOCH₃)CH₃ CH₃ S 1481 OCH₃ SO₂CH₃ CH₃ S 1482 OCH₃ SO₂CF₃ CH₃ S 1483 OCH₃ CH₂CO₂H CH₃ S 1484 OCH₃ CH₂COOCH₃ CH₃ S 1485 OCH₃ CH₂COOC₂H₅ CH₃ S 1486 OCH₃ prop-1-en-3-yl CH₃ S 1487 OCH₃ trans-but-2-en-1-yl CH₃ S 1488 OCH₃ cis-but-2-en-1-yl CH₃ S 1489 OCH₃ cis-3-methyl- CH₃ S but-2-en-1-yl 1490 OCH₃ cyclopropyl CH₃ S 1491 OCH₃ cyclopentyl CH₃ S 1492 OCH₃ cyclohexyl CH₃ S 1493 OCH₃ 4,5-dihydroisoxazol- CH₃ S 3-yl 1494 OCH₃ 4-methyl-4,5-dihydro- CH₃ S isoxazol-3-yl 1495 OCH₃ isoxazol-3-yl CH₃ S 1496 OCH₃ 4-methylisoxazol-3-yl CH₃ S 1497 OCH₃ 4,5-dihydroisoxazol- CH₃ S 4-yl 1498 OCH₃ 3-methyl-4,5-dihydro- CH₃ S isoxazol-4-yl 1499 OCH₃ isoxazol-4-yl CH₃ S 1500 OCH₃ 3-methylisoxazol-4-yl CH₃ S 1501 OCH₃ phenyl CH₃ S 1502 OCH₃ benzyl CH₃ S 1503 OCH₃ benzoyl CH₃ S 1504 OCH₃ 2-pyridyl CH₃ S 1505 OCH₃ H Cl S 1506 OCH₃ CH₃ Cl S 1507 OCH₃ C₂H₅ Cl S 1508 OCH₃ n-C₃H₇ Cl S 1509 OCH₃ i-C₃H₇ Cl S 1510 OCH₃ n-C₄H₉ Cl S 1511 OCH₃ i-C₄H₉ Cl S 1512 OCH₃ s-C₄H₉ Cl S 1513 OCH₃ t-C₄H₉ Cl S 1514 OCH₃ CH₂OCH₃ Cl S 1515 OCH₃ CF₃ Cl S 1516 OCH₃ CF₂H Cl S 1517 OCH₃ CN Cl S 1518 OCH₃ OH Cl S 1519 OCH₃ OCH₃ Cl S 1520 OCH₃ NH₂ Cl S 1521 OCH₃ NHCH₃ Cl S 1522 OCH₃ N(CH₃)₂ Cl S 1523 OCH₃ CO₂CH₃ Cl S 1524 OCH₃ CO₂C₂H₅ Cl S 1525 OCH₃ C(O)CH₃ Cl S 1526 OCH₃ C(O)CF₃ Cl S 1527 OCH₃ C(═NOCH₃)CH₃ Cl S 1528 OCH₃ SO₂CH₃ Cl S 1529 OCH₃ SO₂CF₃ Cl S 1530 OCH₃ CH₂CO₂H Cl S 1531 OCH₃ CH₂COOCH₃ Cl S 1532 OCH₃ CH₂COOC₂H₅ Cl S 1533 OCH₃ prop-1-en-3-yl Cl S 1534 OCH₃ trans-but-2-en-1-yl Cl S 1535 OCH₃ cis-but-2-en-1-yl Cl S 1536 OCH₃ cis-3-methyl- Cl S but-2-en-1-yl 1537 OCH₃ cyclopropyl Cl S 1538 OCH₃ cyclopentyl Cl S 1539 OCH₃ cyclohexyl Cl S 1540 OCH₃ 4,5-dihydroisoxazol- Cl S 3-yl 1541 OCH₃ 4-methyl-4,5-dihydro- Cl S isoxazol-3-yl 1542 OCH₃ isoxazol-3-yl Cl S 1543 OCH₃ 4-methylisoxazol-3-yl Cl S 1544 OCH₃ 4,5-dihydroisoxazol- Cl S 4-yl 1545 OCH₃ 3-methyl-4,5-dihydro- Cl S isoxazol-4-yl 1546 OCH₃ isoxazol-4-yl Cl S 1547 OCH₃ 3-methylisoxazol-4-yl Cl S 1548 OCH₃ phenyl Cl S 1549 OCH₃ benzyl Cl S 1550 OCH₃ benzoyl Cl S 1551 OCH₃ 2-pyridyl Cl S 1552 OCF₃ H H S 1553 OCF₃ CH₃ H S 1554 OCF₃ C₂H₅ H S 1555 OCF₃ n-C₃H₇ H S 1556 OCF₃ i-C₃H₇ H S 1557 OCF₃ n-C₄H₉ H S 1558 OCF₃ i-C₄H₉ H S 1559 OCF₃ s-C₄H₉ H S 1560 OCF₃ t-C₄H₉ H S 1561 OCF₃ CH₂OCH₃ H S 1562 OCF₃ CF₃ H S 1563 OCF₃ CF₂H H S 1564 OCF₃ CN H S 1565 OCF₃ OH H S 1566 OCF₃ OCH₃ H S 1567 OCF₃ NH₂ H S 1568 OCF₃ NHCH₃ H S 1569 OCF₃ N(CH₃)₂ H S 1570 OCF₃ CO₂CH₃ H S 1571 OCF₃ CO₂C₂H₅ H S 1572 OCF₃ C(O)CH₃ H S 1573 OCF₃ C(O)CF₃ H S 1574 OCF₃ C(═NOCH₃)CH₃ H S 1575 OCF₃ SO₂CH₃ H S 1576 OCF₃ SO₂CF₃ H S 1577 OCF₃ CH₂CO₂H H S 1578 OCF₃ CH₂COOCH₃ H S 1579 OCF₃ CH₂COOC₂H₅ H S 1580 OCF₃ prop-1-en-3-yl H S 1581 OCF₃ trans-but-2-en-1-yl H S 1582 OCF₃ cis-but-2-en-1-yl H S 1583 OCF₃ cis-3-methyl- H S but-2-en-1-yl 1584 OCF₃ cyclopropyl H S 1585 OCF₃ cyclopentyl H S 1586 OCF₃ cyclohexyl H S 1587 OCF₃ 4,5-dihydroisoxazol- H S 3-yl 1588 OCF₃ 4-methyl-4,5-dihydro- H S isoxazol-3-yl 1589 OCF₃ isoxazol-3-yl H S 1590 OCF₃ 4-methylisoxazol-3-yl H S 1591 OCF₃ 4,5-dihydroisoxazol- H S 4-yl 1592 OCF₃ 3-methyl-4,5-dihydro- H S isoxazol-4-yl 1593 OCF₃ isoxazol-4-yl H S 1594 OCF₃ 3-methylisoxazol-4-yl H S 1595 OCF₃ phenyl H S 1596 OCF₃ benzyl H S 1597 OCF₃ benzoyl H S 1598 OCF₃ 2-pyridyl H S 1599 OCF₃ H CH₃ S 1600 OCF₃ CH₃ CH₃ S 1601 OCF₃ C₂H₅ CH₃ S 1602 OCF₃ n-C₃H₇ CH₃ S 1603 OCF₃ i-C₃H₇ CH₃ S 1604 OCF₃ n-C₄H₉ CH₃ S 1605 OCF₃ i-C₄H₉ CH₃ S 1606 OCF₃ s-C₄H₉ CH₃ S 1607 OCF₃ t-C₄H₉ CH₃ S 1608 OCF₃ CH₂OCH₃ CH₃ S 1609 OCF₃ CF₃ CH₃ S 1610 OCF₃ CF₂H CH₃ S 1611 OCF₃ CN CH₃ S 1612 OCF₃ OH CH₃ S 1613 OCF₃ OCH₃ CH₃ S 1614 OCF₃ NH₂ CH₃ S 1615 OCF₃ NHCH₃ CH₃ S 1616 OCF₃ N(CH₃)₂ CH₃ S 1617 OCF₃ CO₂CH₃ CH₃ S 1618 OCF₃ CO₂C₂H₅ CH₃ S 1619 OCF₃ C(O)CH₃ CH₃ S 1620 OCF₃ C(O)CF₃ CH₃ S 1621 OCF₃ C(═NOCH₃)CH₃ CH₃ S 1622 OCF₃ SO₂CH₃ CH₃ S 1623 OCF₃ SO₂CF₃ CH₃ S 1624 OCF₃ CH₂CO₂H CH₃ S 1625 OCF₃ CH₂COOCH₃ CH₃ S 1626 OCF₃ CH₂COOC₂H₅ CH₃ S 1627 OCF₃ prop-1-en-3-yl CH₃ S 1628 OCF₃ trans-but-2-en-1-yl CH₃ S 1629 OCF₃ cis-but-2-en-1-yl CH₃ S 1630 OCF₃ cis-3-methyl- CH₃ S but-2-en-1-yl 1631 OCF₃ cyclopropyl CH₃ S 1632 OCF₃ cyclopentyl CH₃ S 1633 OCF₃ cyclohexyl CH₃ S 1634 OCF₃ 4,5-dihydroisoxazol- CH₃ S 3-yl 1635 OCF₃ 4-methyl-4,5-dihydro- CH₃ S isoxazol-3-yl 1636 OCF₃ isoxazol-3-yl CH₃ S 1637 OCF₃ 4-methylisoxazol-3-yl CH₃ S 1638 OCF₃ 4,5-dihydroisoxazol- CH₃ S 4-yl 1639 OCF₃ 3-methyl-4,5-dihydro- CH₃ S isoxazol-4-yl 1640 OCF₃ isoxazol-4-yl CH₃ S 1641 OCF₃ 3-methylisoxazol-4-yl CH₃ S 1642 OCF₃ phenyl CH₃ S 1643 OCF₃ benzyl CH₃ S 1644 OCF₃ benzoyl CH₃ S 1645 OCF₃ 2-pyridyl CH₃ S 1646 OCF₃ H Cl S 1647 OCF₃ CH₃ Cl S 1648 OCF₃ C₂H₅ Cl S 1649 OCF₃ n-C₃H₇ Cl S 1650 OCF₃ i-C₃H₇ Cl S 1651 OCF₃ n-C₄H₉ Cl S 1652 OCF₃ i-C₄H₉ Cl S 1653 OCF₃ s-C₄H₉ Cl S 1654 OCF₃ t-C₄H₉ Cl S 1655 OCF₃ CH₂OCH₃ Cl S 1656 OCF₃ CF₃ Cl S 1657 OCF₃ CF₂H Cl S 1658 OCF₃ CN Cl S 1659 OCF₃ OH Cl S 1660 OCF₃ OCH₃ Cl S 1661 OCF₃ NH₂ Cl S 1662 OCF₃ NHCH₃ Cl S 1663 OCF₃ N(CH₃)₂ Cl S 1664 OCF₃ CO₂CH₃ Cl S 1665 OCF₃ CO₂C₂H₅ Cl S 1666 OCF₃ C(O)CH₃ Cl S 1667 OCF₃ C(O)CF₃ Cl S 1668 OCF₃ C(═NOCH₃)CH₃ Cl S 1669 OCF₃ SO₂CH₃ Cl S 1670 OCF₃ SO₂CF₃ Cl S 1671 OCF₃ CH₂CO₂H Cl S 1672 OCF₃ CH₂COOCH₃ Cl S 1673 OCF₃ CH₂COOC₂H₅ Cl S 1674 OCF₃ prop-1-en-3-yl Cl S 1675 OCF₃ trans-but-2-en-1-yl Cl S 1676 OCF₃ cis-but-2-en-1-yl Cl S 1677 OCF₃ cis-3-methyl- Cl S but-2-en-1-yl 1678 OCF₃ cyclopropyl Cl S 1679 OCF₃ cyclopentyl Cl S 1680 OCF₃ cyclohexyl Cl S 1681 OCF₃ 4,5-dihydroisoxazol- Cl S 3-yl 1682 OCF₃ 4-methyl-4,5-dihydro- Cl S isoxazol-3-yl 1683 OCF₃ isoxazol-3-yl Cl S 1684 OCF₃ 4-methylisoxazol-3-yl Cl S 1685 OCF₃ 4,5-dihydroisoxazol- Cl S 4-yl 1686 OCF₃ 3-methyl-4,5-dihydro- Cl S isoxazol-4-yl 1687 OCF₃ isoxazol-4-yl Cl S 1688 OCF₃ 3-methylisoxazol-4-yl Cl S 1689 OCF₃ phenyl Cl S 1690 OCF₃ benzyl Cl S 1691 OCF₃ benzoyl Cl S 1692 OCF₃ 2-pyridyl Cl S 1693 SCH₃ H H S 1694 SCH₃ CH₃ H S 1695 SCH₃ C₂H₅ H S 1696 SCH₃ n-C₃H₇ H S 1697 SCH₃ i-C₃H₇ H S 1698 SCH₃ n-C₄H₉ H S 1699 SCH₃ i-C₄H₉ H S 1700 SCH₃ s-C₄H₉ H S 1701 SCH₃ t-C₄H₉ H S 1702 SCH₃ CH₂OCH₃ H S 1703 SCH₃ CF₃ H S 1704 SCH₃ CF₂H H S 1705 SCH₃ CN H S 1706 SCH₃ OH H S 1707 SCH₃ OCH₃ H S 1708 SCH₃ NH₂ H S 1709 SCH₃ NHCH₃ H S 1710 SCH₃ N(CH₃)₂ H S 1711 SCH₃ CO₂CH₃ H S 1712 SCH₃ CO₂C₂H₅ H S 1713 SCH₃ C(O)CH₃ H S 1714 SCH₃ C(O)CF₃ H S 1715 SCH₃ C(═NOCH₃)CH₃ H S 1716 SCH₃ SO₂CH₃ H S 1717 SCH₃ SO₂CF₃ H S 1718 SCH₃ CH₂CO₂H H S 1719 SCH₃ CH₂COOCH₃ H S 1720 SCH₃ CH₂COOC₂H₅ H S 1721 SCH₃ prop-1-en-3-yl H S 1722 SCH₃ trans-but-2-en-1-yl H S 1723 SCH₃ cis-but-2-en-1-yl H S 1724 SCH₃ cis-3-methyl- H S but-2-en-1-yl 1725 SCH₃ cyclopropyl H S 1726 SCH₃ cyclopentyl H S 1727 SCH₃ cyclohexyl H S 1728 SCH₃ 4,5-dihydroisoxazol- H S 3-yl 1729 SCH₃ 4-methyl-4,5-dihydro- H S isoxazol-3-yl 1730 SCH₃ isoxazol-3-yl H S 1731 SCH₃ 4-methylisoxazol-3-yl H S 1732 SCH₃ 4,5-dihydroisoxazol- H S 4-yl 1733 SCH₃ 3-methyl-4,5-dihydro- H S isoxazol-4-yl 1734 SCH₃ isoxazol-4-yl H S 1735 SCH₃ 3-methylisoxazol-4-yl H S 1736 SCH₃ phenyl H S 1737 SCH₃ benzyl H S 1738 SCH₃ benzoyl H S 1739 SCH₃ 2-pyridyl H S 1740 SCH₃ H CH₃ S 1741 SCH₃ CH₃ CH₃ S 1742 SCH₃ C₂H₅ CH₃ S 1743 SCH₃ n-C₃H₇ CH₃ S 1744 SCH₃ i-C₃H₇ CH₃ S 1745 SCH₃ n-C₄H₉ CH₃ S 1746 SCH₃ i-C₄H₉ CH₃ S 1747 SCH₃ s-C₄H₉ CH₃ S 1748 SCH₃ t-C₄H₉ CH₃ S 1749 SCH₃ CH₂OCH₃ CH₃ S 1750 SCH₃ CF₃ CH₃ S 1751 SCH₃ CF₂H CH₃ S 1752 SCH₃ CN CH₃ S 1753 SCH₃ OH CH₃ S 1754 SCH₃ OCH₃ CH₃ S 1755 SCH₃ NH₂ CH₃ S 1756 SCH₃ NHCH₃ CH₃ S 1757 SCH₃ N(CH₃)₂ CH₃ S 1758 SCH₃ CO₂CH₃ CH₃ S 1759 SCH₃ CO₂C₂H₅ CH₃ S 1760 SCH₃ C(O)CH₃ CH₃ S 1761 SCH₃ C(O)CF₃ CH₃ S 1762 SCH₃ C(═NOCH₃)CH₃ CH₃ S 1763 SCH₃ SO₂CH₃ CH₃ S 1764 SCH₃ SO₂CF₃ CH₃ S 1765 SCH₃ CH₂CO₂H CH₃ S 1766 SCH₃ CH₂COOCH₃ CH₃ S 1767 SCH₃ CH₂COOC₂H₅ CH₃ S 1768 SCH₃ prop-1-en-3-yl CH₃ S 1769 SCH₃ trans-but-2-en-1-yl CH₃ S 1770 SCH₃ cis-but-2-en-1-yl CH₃ S 1771 SCH₃ cis-3-methyl- CH₃ S but-2-en-1-yl 1772 SCH₃ cyclopropyl CH₃ S 1773 SCH₃ cyclopentyl CH₃ S 1774 SCH₃ cyclohexyl CH₃ S 1775 SCH₃ 4,5-dihydroisoxazol- CH₃ S 3-yl 1776 SCH₃ 4-methyl-4,5-dihydro- CH₃ S isoxazol-3-yl 1777 SCH₃ isoxazol-3-yl CH₃ S 1778 SCH₃ 4-methylisoxazol-3-yl CH₃ S 1779 SCH₃ 4,5-dihydroisoxazol- CH₃ S 4-yl 1780 SCH₃ 3-methyl-4,5-dihydro- CH₃ S isoxazol-4-yl 1781 SCH₃ isoxazol-4-yl CH₃ S 1782 SCH₃ 3-methylisoxazol-4-yl CH₃ S 1783 SCH₃ phenyl CH₃ S 1784 SCH₃ benzyl CH₃ S 1785 SCH₃ benzoyl CH₃ S 1786 SCH₃ 2-pyridyl CH₃ S 1787 SCH₃ H Cl S 1788 SCH₃ CH₃ Cl S 1789 SCH₃ C₂H₅ Cl S 1790 SCH₃ n-C₃H₇ Cl S 1791 SCH₃ i-C₃H₇ Cl S 1792 SCH₃ n-C₄H₉ Cl S 1793 SCH₃ i-C₄H₉ Cl S 1794 SCH₃ s-C₄H₉ Cl S 1795 SCH₃ t-C₄H₉ Cl S 1796 SCH₃ CH₂OCH₃ Cl S 1797 SCH₃ CF₃ Cl S 1798 SCH₃ CF₂H Cl S 1799 SCH₃ CN Cl S 1800 SCH₃ OH Cl S 1801 SCH₃ OCH₃ Cl S 1802 SCH₃ NH₂ Cl S 1803 SCH₃ NHCH₃ Cl S 1804 SCH₃ N(CH₃)₂ Cl S 1805 SCH₃ CO₂CH₃ Cl S 1806 SCH₃ CO₂C₂H₅ Cl S 1807 SCH₃ C(O)CH₃ Cl S 1808 SCH₃ C(O)CF₃ Cl S 1809 SCH₃ C(═NOCH₃)CH₃ Cl S 1810 SCH₃ SO₂CH₃ Cl S 1811 SCH₃ SO₂CF₃ Cl S 1812 SCH₃ CH₂CO₂H Cl S 1813 SCH₃ CH₂COOCH₃ Cl S 1814 SCH₃ CH₂COOC₂H₅ Cl S 1815 SCH₃ prop-1-en-3-yl Cl S 1816 SCH₃ trans-but-2-en-1-yl Cl S 1817 SCH₃ cis-but-2-en-1-yl Cl S 1818 SCH₃ cis-3-methyl- Cl S but-2-en-1-yl 1819 SCH₃ cyclopropyl Cl S 1820 SCH₃ cyclopentyl Cl S 1821 SCH₃ cyclohexyl Cl S 1822 SCH₃ 4,5-dihydroisoxazol- Cl S 3-yl 1823 SCH₃ 4-methyl-4,5-dihydro- Cl S isoxazol-3-yl 1824 SCH₃ isoxazol-3-yl Cl S 1825 SCH₃ 4-methylisoxazol-3-yl Cl S 1826 SCH₃ 4,5-dihydroisoxazol- Cl S 4-yl 1827 SCH₃ 3-methyl-4,5-dihydro- Cl S isoxazol-4-yl 1828 SCH₃ isoxazol-4-yl Cl S 1829 SCH₃ 3-methylisoxazol-4-yl Cl S 1830 SCH₃ phenyl Cl S 1831 SCH₃ benzyl Cl S 1832 SCH₃ benzoyl Cl S 1833 SCH₃ 2-pyridyl Cl S 1834 SO₂CH₃ H H S 1835 SO₂CH₃ CH₃ H S 1836 SO₂CH₃ C₂H₅ H S 1837 SO₂CH₃ n-C₃H₇ H S 1838 SO₂CH₃ i-C₃H₇ H S 1839 SO₂CH₃ n-C₄H₉ H S 1840 SO₂CH₃ i-C₄H₉ H S 1841 SO₂CH₃ s-C₄H₉ H S 1842 SO₂CH₃ t-C₄H₉ H S 1843 SO₂CH₃ CH₂OCH₃ H S 1844 SO₂CH₃ CF₃ H S 1845 SO₂CH₃ CF₂H H S 1846 SO₂CH₃ CN H S 1847 SO₂CH₃ OH H S 1848 SO₂CH₃ OCH₃ H S 1849 SO₂CH₃ NH₂ H S 1850 SO₂CH₃ NHCH₃ H S 1851 SO₂CH₃ N(CH₃)₂ H S 1852 SO₂CH₃ CO₂CH₃ H S 1853 SO₂CH₃ CO₂C₂H₅ H S 1854 SO₂CH₃ C(O)CH₃ H S 1855 SO₂CH₃ C(O)CF₃ H S 1856 SO₂CH₃ C(═NOCH₃)CH₃ H S 1857 SO₂CH₃ SO₂CH₃ H S 1858 SO₂CH₃ SO₂CF₃ H S 1859 SO₂CH₃ CH₂CO₂H H S 1860 SO₂CH₃ CH₂COOCH₃ H S 1861 SO₂CH₃ CH₂COOC₂H₅ H S 1862 SO₂CH₃ prop-1-en-3-yl H S 1863 SO₂CH₃ trans-but-2-en-1-yl H S 1864 SO₂CH₃ cis-but-2-en-1-yl H S 1865 SO₂CH₃ cis-3-methyl- H S but-2-en-1-yl 1866 SO₂CH₃ cyclopropyl H S 1867 SO₂CH₃ cyclopentyl H S 1868 SO₂CH₃ cyclohexyl H S 1869 SO₂CH₃ 4,5-dihydroisoxazol- H S 3-yl 1870 SO₂CH₃ 4-methyl-4,5-dihydro- H S isoxazol-3-yl 1871 SO₂CH₃ isoxazol-3-yl H S 1872 SO₂CH₃ 4-methylisoxazol-3-yl H S 1873 SO₂CH₃ 4,5-dihydroisoxazol- H S 4-yl 1874 SO₂CH₃ 3-methyl-4,5-dihydro- H S isoxazol-4-yl 1875 SO₂CH₃ isoxazol-4-yl H S 1876 SO₂CH₃ 3-methylisoxazol-4-yl H S 1877 SO₂CH₃ phenyl H S 1878 SO₂CH₃ benzyl H S 1879 SO₂CH₃ benzoyl H S 1880 SO₂CH₃ 2-pyridyl H S 1881 SO₂CH₃ H CH₃ S 1882 SO₂CH₃ CH₃ CH₃ S 1883 SO₂CH₃ C₂H₅ CH₃ S 1884 SO₂CH₃ n-C₃H₇ CH₃ S 1885 SO₂CH₃ i-C₃H₇ CH₃ S 1886 SO₂CH₃ n-C₄H₉ CH₃ S 1887 SO₂CH₃ i-C₄H₉ CH₃ S 1888 SO₂CH₃ s-C₄H₉ CH₃ S 1889 SO₂CH₃ t-C₄H₉ CH₃ S 1890 SO₂CH₃ CH₂OCH₃ CH₃ S 1891 SO₂CH₃ CF₃ CH₃ S 1892 SO₂CH₃ CF₂H CH₃ S 1893 SO₂CH₃ CN CH₃ S 1894 SO₂CH₃ OH CH₃ S 1895 SO₂CH₃ OCH₃ CH₃ S 1896 SO₂CH₃ NH₂ CH₃ S 1897 SO₂CH₃ NHCH₃ CH₃ S 1898 SO₂CH₃ N(CH₃)₂ CH₃ S 1899 SO₂CH₃ CO₂CH₃ CH₃ S 1900 SO₂CH₃ CO₂C₂H₅ CH₃ S 1901 SO₂CH₃ C(O)CH₃ CH₃ S 1902 SO₂CH₃ C(O)CF₃ CH₃ S 1903 SO₂CH₃ C(═NOCH₃)CH₃ CH₃ S 1904 SO₂CH₃ SO₂CH₃ CH₃ S 1905 SO₂CH₃ SO₂CF₃ CH₃ S 1906 SO₂CH₃ CH₂CO₂H CH₃ S 1907 SO₂CH₃ CH₂COOCH₃ CH₃ S 1908 SO₂CH₃ CH₂COOC₂H₅ CH₃ S 1909 SO₂CH₃ prop-1-en-3-yl CH₃ S 1910 SO₂CH₃ trans-but-2-en-1-yl CH₃ S 1911 SO₂CH₃ cis-but-2-en-1-yl CH₃ S 1912 SO₂CH₃ cis-3-methyl- CH₃ S but-2-en-1-yl 1913 SO₂CH₃ cyclopropyl CH₃ S 1914 SO₂CH₃ cyclopentyl CH₃ S 1915 SO₂CH₃ cyclohexyl CH₃ S 1916 SO₂CH₃ 4,5-dihydroisoxazol- CH₃ S 3-yl 1917 SO₂CH₃ 4-methyl-4,5-dihydro- CH₃ S isoxazol-3-yl 1918 SO₂CH₃ isoxazol-3-yl CH₃ S 1919 SO₂CH₃ 4-methylisoxazol-3-yl CH₃ S 1920 SO₂CH₃ 4,5-dihydroisoxazol- CH₃ S 4-yl 1921 SO₂CH₃ 3-methyl-4,5-dihydro- CH₃ S isoxazol-4-yl 1922 SO₂CH₃ isoxazol-4-yl CH₃ S 1923 SO₂CH₃ 3-methylisoxazol-4-yl CH₃ S 1924 SO₂CH₃ phenyl CH₃ S 1925 SO₂CH₃ benzyl CH₃ S 1926 SO₂CH₃ benzoyl CH₃ S 1927 SO₂CH₃ 2-pyridyl CH₃ S 1928 SO₂CH₃ H Cl S 1929 SO₂CH₃ CH₃ Cl S 1930 SO₂CH₃ C₂H₅ Cl S 1931 SO₂CH₃ n-C₃H₇ Cl S 1932 SO₂CH₃ i-C₃H₇ Cl S 1933 SO₂CH₃ n-C₄H₉ Cl S 1934 SO₂CH₃ i-C₄H₉ Cl S 1935 SO₂CH₃ s-C₄H₉ Cl S 1936 SO₂CH₃ t-C₄H₉ Cl S 1937 SO₂CH₃ CH₂OCH₃ Cl S 1938 SO₂CH₃ CF₃ Cl S 1939 SO₂CH₃ CF₂H Cl S 1940 SO₂CH₃ CN Cl S 1941 SO₂CH₃ OH Cl S 1942 SO₂CH₃ OCH₃ Cl S 1943 SO₂CH₃ NH₂ Cl S 1944 SO₂CH₃ NHCH₃ Cl S 1945 SO₂CH₃ N(CH₃)₂ Cl S 1946 SO₂CH₃ CO₂CH₃ Cl S 1947 SO₂CH₃ CO₂C₂H₅ Cl S 1948 SO₂CH₃ C(O)CH₃ Cl S 1949 SO₂CH₃ C(O)CF₃ Cl S 1950 SO₂CH₃ C(═NOCH₃)CH₃ Cl S 1951 SO₂CH₃ SO₂CH₃ Cl S 1952 SO₂CH₃ SO₂CF₃ Cl S 1953 SO₂CH₃ CH₂CO₂H Cl S 1954 SO₂CH₃ CH₂COOCH₃ Cl S 1955 SO₂CH₃ CH₂COOC₂H₅ Cl S 1956 SO₂CH₃ prop-1-en-3-yl Cl S 1957 SO₂CH₃ trans-but-2-en-1-yl Cl S 1958 SO₂CH₃ cis-but-2-en-1-yl Cl S 1959 SO₂CH₃ cis-3-methyl- Cl S but-2-en-1-yl 1960 SO₂CH₃ cyclopropyl Cl S 1961 SO₂CH₃ cyclopentyl Cl S 1962 SO₂CH₃ cyclohexyl Cl S 1963 SO₂CH₃ 4,5-dihydroisoxazol- Cl S 3-yl 1964 SO₂CH₃ 4-methyl-4,5-dihydro- Cl S isoxazol-3-yl 1965 SO₂CH₃ isoxazol-3-yl Cl S 1966 SO₂CH₃ 4-methylisoxazol-3-yl Cl S 1967 SO₂CH₃ 4,5-dihydroisoxazol- Cl S 4-yl 1968 SO₂CH₃ 3-methyl-4,5-dihydro- Cl S isoxazol-4-yl 1969 SO₂CH₃ isoxazol-4-yl Cl S 1970 SO₂CH₃ 3-methylisoxazol-4-yl Cl S 1971 SO₂CH₃ phenyl Cl S 1972 SO₂CH₃ benzyl Cl S 1973 SO₂CH₃ benzoyl Cl S 1974 SO₂CH₃ 2-pyridyl Cl S 1975 CF₃ H H S 1976 CF₃ CH₃ H S 1977 CF₃ C₂H₅ H S 1978 CF₃ n-C₃H₇ H S 1979 CF₃ i-C₃H₇ H S 1980 CF₃ n-C₄H₉ H S 1981 CF₃ i-C₄H₉ H S 1982 CF₃ s-C₄H₉ H S 1983 CF₃ t-C₄H₉ H S 1984 CF₃ CH₂OCH₃ H S 1985 CF₃ CF₃ H S 1986 CF₃ CF₂H H S 1987 CF₃ CN H S 1988 CF₃ OH H S 1989 CF₃ OCH₃ H S 1990 CF₃ NH₂ H S 1991 CF₃ NHCH₃ H S 1992 CF₃ N(CH₃)₂ H S 1993 CF₃ CO₂CH₃ H S 1994 CF₃ CO₂C₂H₅ H S 1995 CF₃ C(O)CH₃ H S 1996 CF₃ C(O)CF₃ H S 1997 CF₃ C(═NOCH₃)CH₃ H S 1998 CF₃ SO₂CH₃ H S 1999 CF₃ SO₂CF₃ H S 2000 CF₃ CH₂CO₂H H S 2001 CF₃ CH₂COOCH₃ H S 2002 CF₃ CH₂COOC₂H₅ H S 2003 CF₃ prop-1-en-3-yl H S 2004 CF₃ trans-but-2-en-1-yl H S 2005 CF₃ cis-but-2-en-1-yl H S 2006 CF₃ cis-3-methyl- H S but-2-en-1-yl 2007 CF₃ cyclopropyl H S 2008 CF₃ cyclopentyl H S 2009 CF₃ cyclohexyl H S 2010 CF₃ 4,5-dihydroisoxazol- H S 3-yl 2011 CF₃ 4-methyl-4,5-dihydro- H S isoxazol-3-yl 2012 CF₃ isoxazol-3-yl H S 2013 CF₃ 4-methylisoxazol-3-yl H S 2014 CF₃ 4,5-dihydroisoxazol- H S 4-yl 2015 CF₃ 3-methyl-4,5-dihydro- H isoxazol-4-yl 2016 CF₃ isoxazol-4-yl H S 2017 CF₃ 3-methylisoxazol-4-yl H S 2018 CF₃ phenyl H S 2019 CF₃ benzyl H S 2020 CF₃ benzoyl H S 2021 CF₃ 2-pyridyl H S 2022 CF₃ H CH₃ S 2023 CF₃ CH₃ CH₃ S 2024 CF₃ C₂H₅ CH₃ S 2025 CF₃ n-C₃H₇ CH₃ S 2026 CF₃ i-C₃H₇ CH₃ S 2027 CF₃ n-C₄H₉ CH₃ S 2028 CF₃ i-C₄H₉ CH₃ S 2029 CF₃ s-C₄H₉ CH₃ S 2030 CF₃ t-C₄H₉ CH₃ S 2031 CF₃ CH₂OCH₃ CH₃ S 2032 CF₃ CF₃ CH₃ S 2033 CF₃ CF₂H CH₃ S 2034 CF₃ CN CH₃ S 2035 CF₃ OH CH₃ S 2036 CF₃ OCH₃ CH₃ S 2037 CF₃ NH₂ CH₃ S 2038 CF₃ NHCH₃ CH₃ S 2039 CF₃ N(CH₃)₂ CH₃ S 2040 CF₃ CO₂CH₃ CH₃ S 2041 CF₃ CO₂C₂H₅ CH₃ S 2042 CF₃ C(O)CH₃ CH₃ S 2043 CF₃ C(O)CF₃ CH₃ S 2044 CF₃ C(═NOCH₃)CH₃ CH₃ S 2045 CF₃ SO₂CH₃ CH₃ S 2046 CF₃ SO₂CF₃ CH₃ S 2047 CF₃ CH₂CO₂H CH₃ S 2048 CF₃ CH₂COOCH₃ CH₃ S 2049 CF₃ CH₂COOC₂H₅ CH₃ S 2050 CF₃ prop-1-en-3-yl CH₃ S 2051 CF₃ trans-but-2-en-1-yl CH₃ S 2052 CF₃ cis-but-2-en-1-yl CH₃ S 2053 CF₃ cis-3-methyl- CH₃ S but-2-en-1-yl 2054 CF₃ cyclopropyl CH₃ S 2055 CF₃ cyclopentyl CH₃ S 2056 CF₃ cyclohexyl CH₃ S 2057 CF₃ 4,5-dihydroisoxazol- CH₃ S 3-yl 2058 CF₃ 4-methyl-4,5-dihydro- CH₃ S isoxazol-3-yl 2059 CF₃ isoxazol-3-yl CH₃ S 2060 CF₃ 4-methylisoxazol-3-yl CH₃ S 2061 CF₃ 4,5-dihydroisoxazol- CH₃ S 4-yl 2062 CF₃ 3-methyl-4,5-dihydro- CH₃ S isoxazol-4-yl 2063 CF₃ isoxazol-4-yl CH₃ S 2064 CF₃ 3-methylisoxazol-4-yl CH₃ S 2065 CF₃ phenyl CH₃ S 2066 CF₃ benzyl CH₃ S 2067 CF₃ benzoyl CH₃ S 2068 CF₃ 2-pyridyl CH₃ S 2069 CF₃ H Cl S 2070 CF₃ CH₃ Cl S 2071 CF₃ C₂H₅ Cl S 2072 CF₃ n-C₃H₇ Cl S 2073 CF₃ i-C₃H₇ Cl S 2074 CF₃ n-C₄H₉ Cl S 2075 CF₃ i-C₄H₉ Cl S 2076 CF₃ s-C₄H₉ Cl S 2077 CF₃ t-C₄H₉ Cl S 2078 CF₃ CH₂OCH₃ Cl S 2079 CF₃ CF₃ Cl S 2080 CF₃ CF₂H Cl S 2081 CF₃ CN Cl S 2082 CF₃ OH Cl S 2083 CF₃ OCH₃ Cl S 2084 CF₃ NH₂ Cl S 2085 CF₃ NHCH₃ Cl S 2086 CF₃ N(CH₃)₂ Cl S 2087 CF₃ CO₂CH₃ Cl S 2088 CF₃ CO₂C₂H₅ Cl S 2089 CF₃ C(O)CH₃ Cl S 2090 CF₃ C(O)CF₃ Cl S 2091 CF₃ C(═NOCH₃)CH₃ Cl S 2092 CF₃ SO₂CH₃ Cl S 2093 CF₃ SO₂CF₃ Cl S 2094 CF₃ CH₂CO₂H Cl S 2095 CF₃ CH₂COOCH₃ Cl S 2096 CF₃ CH₂COOC₂H₅ Cl S 2097 CF₃ prop-1-en-3-yl Cl S 2098 CF₃ trans-but-2-en-1-yl Cl S 2099 CF₃ cis-but-2-en-1-yl Cl S 2100 CF₃ cis-3-methyl- Cl S but-2-en-1-yl 2101 CF₃ cyclopropyl Cl S 2102 CF₃ cyclopentyl Cl S 2103 CF₃ cyclohexyl Cl S 2104 CF₃ 4,5-dihydroisoxazol- Cl S 3-yl 2105 CF₃ 4-methyl-4,5-dihydro- Cl S isoxazol-3-yl 2106 CF₃ isoxazol-3-yl Cl S 2107 CF₃ 4-methylisoxazol-3-yl Cl S 2108 CF₃ 4,5-dihydroisoxazol- Cl S 4-yl 2109 CF₃ 3-methyl-4,5-dihydro- Cl S isoxazol-4-yl 2110 CF₃ isoxazol-4-yl Cl S 2111 CF₃ 3-methylisoxazol-4-yl Cl S 2112 CF₃ phenyl Cl S 2113 CF₃ benzyl Cl S 2114 CF₃ benzoyl Cl S 2115 CF₃ 2-pyridyl Cl S 2116 C₂H₅ H H S 2117 C₂H₅ CH₃ H S 2118 C₂H₅ C₂H₅ H S 2119 C₂H₅ n-C₃H₇ H S 2120 C₂H₅ i-C₃H₇ H S 2121 C₂H₅ n-C₄H₉ H S 2122 C₂H₅ i-C₄H₉ H S 2123 C₂H₅ s-C₄H₉ H S 2124 C₂H₅ t-C₄H₉ H S 2125 C₂H₅ CH₂OCH₃ H S 2126 C₂H₅ CF₃ H S 2127 C₂H₅ CF₂H H S 2128 C₂H₅ CN H S 2129 C₂H₅ OH H S 2130 C₂H₅ OCH₃ H S 2131 C₂H₅ NH₂ H S 2132 C₂H₅ NHCH₃ H S 2133 C₂H₅ N(CH₃)₂ H S 2134 C₂H₅ CO₂CH₃ H S 2135 C₂H₅ CO₂C₂H₅ H S 2136 C₂H₅ C(O)CH₃ H S 2137 C₂H₅ C(O)CF₃ H S 2138 C₂H₅ C(═NOCH₃)CH₃ H S 2139 C₂H₅ SO₂CH₃ H S 2140 C₂H₅ SO₂CF₃ H S 2141 C₂H₅ CH₂CO₂H H S 2142 C₂H₅ CH₂COOCH₃ H S 2143 C₂H₅ CH₂COOC₂H₅ H S 2144 C₂H₅ prop-1-en-3-yl H S 2145 C₂H₅ trans-but-2-en-1-yl H S 2146 C₂H₅ cis-but-2-en-1-yl H S 2147 C₂H₅ cis-3-methyl- H S but-2-en-1-yl 2148 C₂H₅ cyclopropyl H S 2149 C₂H₅ cyclopentyl H S 2150 C₂H₅ cyclohexyl H S 2151 C₂H₅ 4,5-dihydroisoxazol- H S 3-yl 2152 C₂H₅ 4-methyl-4,5-dihydro- H S isoxazol-3-yl 2153 C₂H₅ isoxazol-3-yl H S 2154 C₂H₅ 4-methylisoxazol-3-yl H S 2155 C₂H₅ 4,5-dihydroisoxazol- H S 4-yl 2156 C₂H₅ 3-methyl-4,5-dihydro- H S isoxazol-4-yl 2157 C₂H₅ isoxazol-4-yl H S 2158 C₂H₅ 3-methylisoxazol-4-yl H S 2159 C₂H₅ phenyl H S 2160 C₂H₅ benzyl H S 2161 C₂H₅ benzoyl H S 2162 C₂H₅ 2-pyridyl H S 2163 C₂H₅ H CH₃ S 2164 C₂H₅ CH₃ CH₃ S 2165 C₂H₅ C₂H₅ CH₃ S 2166 C₂H₅ n-C₃H₇ CH₃ S 2167 C₂H₅ i-C₃H₇ CH₃ S 2168 C₂H₅ n-C₄H₉ CH₃ S 2169 C₂H₅ i-C₄H₉ CH₃ S 2170 C₂H₅ s-C₄H₉ CH₃ S 2171 C₂H₅ t-C₄H₉ CH₃ S 2172 C₂H₅ CH₂OCH₃ CH₃ S 2173 C₂H₅ CF₃ CH₃ S 2174 C₂H₅ CF₂H CH₃ S 2175 C₂H₅ CN CH₃ S 2176 C₂H₅ OH CH₃ S 2177 C₂H₅ OCH₃ CH₃ S 2178 C₂H₅ NH₂ CH₃ S 2179 C₂H₅ NHCH₃ CH₃ S 2180 C₂H₅ N(CH₃)₂ CH₃ S 2181 C₂H₅ CO₂CH₃ CH₃ S 2182 C₂H₅ CO₂C₂H₅ CH₃ S 2183 C₂H₅ C(O)CH₃ CH₃ S 2184 C₂H₅ C(O)CF₃ CH₃ S 2185 C₂H₅ C(═NOCH₃)CH₃ CH₃ S 2186 C₂H₅ SO₂CH₃ CH₃ S 2187 C₂H₅ SO₂CF₃ CH₃ S 2188 C₂H₅ CH₂CO₂H CH₃ S 2189 C₂H₅ CH₂COOCH₃ CH₃ S 2190 C₂H₅ CH₂COOC₂H₅ CH₃ S 2191 C₂H₅ prop-1-en-3-yl CH₃ S 2192 C₂H₅ trans-but-2-en-1-yl CH₃ S 2193 C₂H₅ cis-but-2-en-1-yl CH₃ S 2194 C₂H₅ cis-3-methyl- CH₃ S but-2-en-1-yl 2195 C₂H₅ cyclopropyl CH₃ S 2196 C₂H₅ cyclopentyl CH₃ S 2197 C₂H₅ cyclohexyl CH₃ S 2198 C₂H₅ 4,5-dihydroisoxazol- CH₃ S 3-yl 2199 C₂H₅ 4-methyl-4,5-dihydro- CH₃ S isoxazol-3-yl 2200 C₂H₅ isoxazol-3-yl CH₃ S 2201 C₂H₅ 4-methylisoxazol-3-yl CH₃ S 2202 C₂H₅ 4,5-dihydroisoxazol- CH₃ S 4-yl 2203 C₂H₅ 3-methyl-4,5-dihydro- CH₃ S isoxazol-4-yl 2204 C₂H₅ isoxazol-4-yl CH₃ S 2205 C₂H₅ 3-methylisoxazol-4-yl CH₃ S 2206 C₂H₅ phenyl CH₃ S 2207 C₂H₅ benzyl CH₃ S 2208 C₂H₅ benzoyl CH₃ S 2209 C₂H₅ 2-pyridyl CH₃ S 2210 C₂H₅ H Cl S 2211 C₂H₅ CH₃ Cl S 2212 C₂H₅ C₂H₅ Cl S 2213 C₂H₅ n-C₃H₇ Cl S 2214 C₂H₅ i-C₃H₇ Cl S 2215 C₂H₅ n-C₄H₉ Cl S 2216 C₂H₅ i-C₄H₉ Cl S 2217 C₂H₅ s-C₄H₉ Cl S 2218 C₂H₅ t-C₄H₉ Cl S 2219 C₂H₅ CH₂OCH₃ Cl S 2220 C₂H₅ CF₃ Cl S 2221 C₂H₅ CF₂H Cl S 2222 C₂H₅ CN Cl S 2223 C₂H₅ OH Cl S 2224 C₂H₅ OCH₃ Cl S 2225 C₂H₅ NH₂ Cl S 2226 C₂H₅ NHCH₃ Cl S 2227 C₂H₅ N(CH₃)₂ Cl S 2228 C₂H₅ CO₂CH₃ Cl S 2229 C₂H₅ CO₂C₂H₅ Cl S 2230 C₂H₅ C(O)CH₃ Cl S 2231 C₂H₅ C(O)CF₃ Cl S 2232 C₂H₅ C(═NOCH₃)CH₃ Cl S 2233 C₂H₅ SO₂CH₃ Cl S 2234 C₂H₅ SO₂CF₃ Cl S 2235 C₂H₅ CH₂CO₂H Cl S 2236 C₂H₅ CH₂COOCH₃ Cl S 2237 C₂H₅ CH₂COOC₂H₅ Cl S 2238 C₂H₅ prop-1-en-3-yl Cl S 2239 C₂H₅ trans-but-2-en-1-yl Cl S 2240 C₂H₅ cis-but-2-en-1-yl Cl S 2241 C₂H₅ cis-3-methyl- Cl S but-2-en-1-yl 2242 C₂H₅ cyclopropyl Cl S 2243 C₂H₅ cyclopentyl Cl S 2244 C₂H₅ cyclohexyl Cl S 2245 C₂H₅ 4,5-dihydroisoxazol- Cl S 3-yl 2246 C₂H₅ 4-methyl-4,5-dihydro- Cl S isoxazol-3-yl 2247 C₂H₅ isoxazol-3-yl Cl S 2248 C₂H₅ 4-methylisoxazol-3-yl Cl S 2249 C₂H₅ 4,5-dihydroisoxazol- Cl S 4-yl 2250 C₂H₅ 3-methyl-4,5-dihydro- Cl S isoxazol-4-yl 2251 C₂H₅ isoxazol-4-yl Cl S 2252 C₂H₅ 3-methylisoxazol-4-yl Cl S 2253 C₂H₅ phenyl Cl S 2254 C₂H₅ benzyl Cl S 2255 C₂H₅ benzoyl Cl S 2256 C₂H₅ 2-pyridyl Cl S 2257 CH₃ H H NCH₃ 2258 CH₃ CH₃ H NCH₃ 2259 CH₃ C₂H₅ H NCH₃ 2260 CH₃ n-C₃H₇ H NCH₃ 2261 CH₃ i-C₃H₇ H NCH₃ 2262 CH₃ n-C₄H₉ H NCH₃ 2263 CH₃ i-C₄H₉ H NCH₃ 2264 CH₃ s-C₄H₉ H NCH₃ 2265 CH₃ t-C₄H₉ H NCH₃ 2266 CH₃ CH₂OCH₃ H NCH₃ 2267 CH₃ CF₃ H NCH₃ 2268 CH₃ CF₂H H NCH₃ 2269 CH₃ CN H NCH₃ 2270 CH₃ OH H NCH₃ 2271 CH₃ OCH₃ H NCH₃ 2272 CH₃ NH₂ H NCH₃ 2273 CH₃ NHCH₃ H NCH₃ 2274 CH₃ N(CH₃)₂ H NCH₃ 2275 CH₃ CO₂CH₃ H NCH₃ 2276 CH₃ CO₂C₂H₅ H NCH₃ 2277 CH₃ C(O)CH₃ H NCH₃ 2278 CH₃ C(O)CF₃ H NCH₃ 2279 CH₃ C(═NOCH₃)CH₃ H NCH₃ 2280 CH₃ SO₂CH₃ H NCH₃ 2281 CH₃ SO₂CF₃ H NCH₃ 2282 CH₃ CH₂CO₂H H NCH₃ 2283 CH₃ CH₂COOCH₃ H NCH₃ 2284 CH₃ CH₂COOC₂H₅ H NCH₃ 2285 CH₃ prop-1-en-3-yl H NCH₃ 2286 CH₃ trans-but-2-en-1-yl H NCH₃ 2287 CH₃ cis-but-2-en-1-y1 H NCH₃ 2288 CH₃ cis-3-methyl- H NCH₃ but-2-en-1-yl 2289 CH₃ cyclopropyl H NCH₃ 2290 CH₃ cyclopentyl H NCH₃ 2291 CH₃ cyclohexyl H NCH₃ 2292 CH₃ 4,5-dihydroisoxazol- H NCH₃ 3-yl 2293 CH₃ 4-methyl-4,5-dihydro- H NCH₃ isoxazol-3-yl 2294 CH₃ isoxazol-3-yl H NCH₃ 2295 CH₃ 4-methylisoxazol- H NCH₃ 3-yl 2296 CH₃ 4,5-dihydroisoxazol- H NCH₃ 4-yl 2297 CH₃ 3-methyl-4,5-dihydro- H NCH₃ isoxazol-4-yl 2298 CH₃ isoxazol-4-yl H NCH₃ 2299 CH₃ 3-methylisoxazol- H NCH₃ 4-yl 2300 CH₃ phenyl H NCH₃ 2301 CH₃ benzyl H NCH₃ 2302 CH₃ benzoyl H NCH₃ 2303 CH₃ 2-pyridyl H NCH₃ 2304 CH₃ H CH₃ NCH₃ 2305 CH₃ CH₃ CH₃ NCH₃ 2306 CH₃ C₂H₅ CH₃ NCH₃ 2307 CH₃ n-C₃H₇ CH₃ NCH₃ 2308 CH₃ i-C₃H₇ CH₃ NCH₃ 2309 CH₃ n-C₄H₉ CH₃ NCH₃ 2310 CH₃ i-C₄H₉ CH₃ NCH₃ 2311 CH₃ s-C₄H₉ CH₃ NCH₃ 2312 CH₃ t-C₄H₉ CH₃ NCH₃ 2313 CH₃ CH₂OCH₃ CH₃ NCH₃ 2314 CH₃ CF₃ CH₃ NCH₃ 2315 CH₃ CF₂H CH₃ NCH₃ 2316 CH₃ CN CH₃ NCH₃ 2317 CH₃ OH CH₃ NCH₃ 2318 CH₃ OCH₃ CH₃ NCH₃ 2319 CH₃ NH₂ CH₃ NCH₃ 2320 CH₃ NHCH₃ CH₃ NCH₃ 2321 CH₃ N(CH₃)₂ CH₃ NCH₃ 2322 CH₃ CO₂CH₃ CH₃ NCH₃ 2323 CH₃ CO₂C₂H₅ CH₃ NCH₃ 2324 CH₃ C(O)CH₃ CH₃ NCH₃ 2325 CH₃ C(O)CF₃ CH₃ NCH₃ 2326 CH₃ C(═NOCH₃)CH₃ CH₃ NCH₃ 2327 CH₃ SO₂CH₃ CH₃ NCH₃ 2328 CH₃ SO₂CF₃ CH₃ NCH₃ 2329 CH₃ CH₂CO₂H CH₃ NCH₃ 2330 CH₃ CH₂COOCH₃ CH₃ NCH₃ 2331 CH₃ CH₂COOC₂H₅ CH₃ NCH₃ 2332 CH₃ prop-1-en-3-yl CH₃ NCH₃ 2333 CH₃ trans-but-2-en-1-yl CH₃ NCH₃ 2334 CH₃ cis-but-2-en-1-yl CH₃ NCH₃ 2335 CH₃ cis-3-methyl- CH₃ NCH₃ but-2-en-1-yl 2336 CH₃ cyclopropyl CH₃ NCH₃ 2337 CH₃ cyclopentyl CH₃ NCH₃ 2338 CH₃ cyclohexyl CH₃ NCH₃ 2339 CH₃ 4,5-dihydroisoxazol- CH₃ NCH₃ 3-yl 2340 CH₃ 4-methyl-4,5-dihydro- CH₃ NCH₃ isoxazol-3-yl 2341 CH₃ isoxazol-3-yl CH₃ NCH₃ 2342 CH₃ 4-methylisoxazol-3-yl CH₃ NCH₃ 2343 CH₃ 4,5-dihydroisoxazol- CH₃ NCH₃ 4-yl 2344 CH₃ 3-methyl-4,5-dihydro- CH₃ NCH₃ isoxazol-4-yl 2345 CH₃ isoxazol-4-yl CH₃ NCH₃ 2346 CH₃ 3-methylisoxazol-4-yl CH₃ NCH₃ 2347 CH₃ phenyl CH₃ NCH₃ 2348 CH₃ benzyl CH₃ NCH₃ 2349 CH₃ benzoyl CH₃ NCH₃ 2350 CH₃ 2-pyridyl CH₃ NCH₃ 2351 CH₃ H Cl NCH₃ 2352 CH₃ CH₃ Cl NCH₃ 2353 CH₃ C₂H₅ Cl NCH₃ 2354 CH₃ n-C₃H₇ Cl NCH₃ 2355 CH₃ i-C₃H₇ Cl NCH₃ 2356 CH₃ n-C₄H₉ Cl NCH₃ 2357 CH₃ i-C₄H₉ Cl NCH₃ 2358 CH₃ s-C₄H₉ Cl NCH₃ 2359 CH₃ t-C₄H₉ Cl NCH₃ 2360 CH₃ CH₂OCH₃ Cl NCH₃ 2361 CH₃ CF₃ Cl NCH₃ 2362 CH₃ CF₂H Cl NCH₃ 2363 CH₃ CN Cl NCH₃ 2364 CH₃ OH Cl NCH₃ 2365 CH₃ OCH₃ Cl NCH₃ 2366 CH₃ NH₂ Cl NCH₃ 2367 CH₃ NHCH₃ Cl NCH₃ 2368 CH₃ N(CH₃)₂ Cl NCH₃ 2369 CH₃ CO₂CH₃ Cl NCH₃ 2370 CH₃ CO₂C₂H₅ Cl NCH₃ 2371 CH₃ C(O)CH₃ Cl NCH₃ 2372 CH₃ C(O)CF₃ Cl NCH₃ 2373 CH₃ C(═NOCH₃)CH₃ Cl NCH₃ 2374 CH₃ SO₂CH₃ Cl NCH₃ 2375 CH₃ SO₂CF₃ Cl NCH₃ 2376 CH₃ CH₂CO₂H Cl NCH₃ 2377 CH₃ CH₂COOCH₃ Cl NCH₃ 2378 CH₃ CH₂COOC₂H₅ Cl NCH₃ 2379 CH₃ prop-1-en-3-yl Cl NCH₃ 2380 CH₃ trans-but-2-en-1-yl Cl NCH₃ 2381 CH₃ cis-but-2-en-1-yl Cl NCH₃ 2382 CH₃ cis-3-methyl- Cl NCH₃ but-2-en-1-yl 2383 CH₃ cyclopropyl Cl NCH₃ 2384 CH₃ cyclopentyl Cl NCH₃ 2385 CH₃ cyclohexyl Cl NCH₃ 2386 CH₃ 4,5-dihydroisoxazol- Cl NCH₃ 3-yl 2387 CH₃ 4-methyl-4,5-dihydro- Cl NCH₃ isoxazol-3-yl 2388 CH₃ isoxazol-3-yl Cl NCH₃ 2389 CH₃ 4-methylisoxazol-3-yl Cl NCH₃ 2390 CH₃ 4,5-dihydroisoxazol- Cl NCH₃ 4-yl 2391 CH₃ 3-methyl-4,5-dihydro- Cl NCH₃ isoxazol-4-yl 2392 CH₃ isoxazol-4-yl Cl NCH₃ 2393 CH₃ 3-methylisoxazol-4-yl Cl NCH₃ 2394 CH₃ phenyl Cl NCH₃ 2395 CH₃ benzyl Cl NCH₃ 2396 CH₃ benzoyl Cl NCH₃ 2397 CH₃ 2-pyridyl Cl NCH₃ 2398 Cl H H NCH₃ 2399 Cl CH₃ H NCH₃ 2400 Cl C₂H₅ H NCH₃ 2401 Cl n-C₃H₇ H NCH₃ 2402 Cl i-C₃H₇ H NCH₃ 2403 Cl n-C₄H₉ H NCH₃ 2404 Cl i-C₄H₉ H NCH₃ 2405 Cl s-C₄H₉ H NCH₃ 2406 Cl t-C₄H₉ H NCH₃ 2407 Cl CH₂OCH₃ H NCH₃ 2408 Cl CF₃ H NCH₃ 2409 Cl CF₂H H NCH₃ 2410 Cl CN H NCH₃ 2411 Cl OH H NCH₃ 2412 Cl OCH₃ H NCH₃ 2413 Cl NH₂ H NCH₃ 2414 Cl NHCH₃ H NCH₃ 2415 Cl N(CH₃)₂ H NCH₃ 2416 Cl CO₂CH₃ H NCH₃ 2417 Cl CO₂C₂H₅ H NCH₃ 2418 Cl C(O)CH₃ H NCH₃ 2419 Cl C(O)CF₃ H NCH₃ 2420 Cl C(═NOCH₃)CH₃ H NCH₃ 2421 Cl SO₂CH₃ H NCH₃ 2422 Cl SO₂CF₃ H NCH₃ 2423 Cl CH₂CO₂H H NCH₃ 2424 Cl CH₂COOCH₃ H NCH₃ 2425 Cl CH₂COOC₂H₅ H NCH₃ 2426 Cl prop-1-en-3-yl H NCH₃ 2427 Cl trans-but-2-en-1-yl H NCH₃ 2428 Cl cis-but-2-en-1-yl H NCH₃ 2429 Cl cis-3-methyl- H NCH₃ but-2-en-1-yl 2430 Cl cyclopropyl H NCH₃ 2431 Cl cyclopentyl H NCH₃ 2432 Cl cyclohexyl H NCH₃ 2433 Cl 4,5-dihydroisoxazol- H NCH₃ 3-yl 2434 Cl 4-methyl-4,5-dihydro- H NCH₃ isoxazol-3-yl 2435 Cl isoxazol-3-yl H NCH₃ 2436 Cl 4-methylisoxazol-3-yl H NCH₃ 2437 Cl 4,5-dihydroisoxazol- H NCH₃ 4-yl 2438 Cl 3-methyl-4,5-dihydro- H NCH₃ isoxazol-4-yl 2439 Cl isoxazol-4-yl H NCH₃ 2440 Cl 3-methylisoxazol-4-yl H NCH₃ 2441 Cl phenyl H NCH₃ 2442 Cl benzyl H NCH₃ 2443 Cl benzoyl H NCH₃ 2444 Cl 2-pyridyl H NCH₃ 2445 Cl H CH₃ NCH₃ 2446 Cl CH₃ CH₃ NCH₃ 2447 Cl C₂H₅ CH₃ NCH₃ 2448 Cl n-C₃H₇ CH₃ NCH₃ 2449 Cl i-C₃H₇ CH₃ NCH₃ 2450 Cl n-C₄H₉ CH₃ NCH₃ 2451 Cl i-C₄H₉ CH₃ NCH₃ 2452 Cl s-C₄H₉ CH₃ NCH₃ 2453 Cl t-C₄H₉ CH₃ NCH₃ 2454 Cl CH₂OCH₃ CH₃ NCH₃ 2455 Cl CF₃ CH₃ NCH₃ 2456 Cl CF₂H CH₃ NCH₃ 2457 Cl CN CH₃ NCH₃ 2458 Cl OH CH₃ NCH₃ 2459 Cl OCH₃ CH₃ NCH₃ 2460 Cl NH₂ CH₃ NCH₃ 2461 Cl NHCH₃ CH₃ NCH₃ 2462 Cl N(CH₃)₂ CH₃ NCH₃ 2463 Cl CO₂CH₃ CH₃ NCH₃ 2464 Cl CO₂C₂H₅ CH₃ NCH₃ 2465 Cl C(O)CH₃ CH₃ NCH₃ 2466 Cl C(O)CF₃ CH₃ NCH₃ 2467 Cl C(═NOCH₃)CH₃ CH₃ NCH₃ 2468 Cl SO₂CH₃ CH₃ NCH₃ 2469 Cl SO₂CF₃ CH₃ NCH₃ 2470 Cl CH₂CO₂H CH₃ NCH₃ 2471 Cl CH₂COOCH₃ CH₃ NCH₃ 2472 Cl CH₂COOC₂H₅ CH₃ NCH₃ 2473 Cl prop-1-en-3-yl CH₃ NCH₃ 2474 Cl trans-but-2-en-1-yl CH₃ NCH₃ 2475 Cl cis-but-2-en-1-yl CH₃ NCH₃ 2476 Cl cis-3-methyl- CH₃ NCH₃ but-2-en-1-yl 2477 Cl cyclopropyl CH₃ NCH₃ 2478 Cl cyclopentyl CH₃ NCH₃ 2479 Cl cyclohexyl CH₃ NCH₃ 2480 Cl 4,5-dihydroisoxazol- CH₃ NCH₃ 3-yl 2481 Cl 4-methyl-4,5-dihydro- CH₃ NCH₃ isoxazol-3-yl 2482 Cl isoxazol-3-yl CH₃ NCH₃ 2483 Cl 4-methylisoxazol-3-yl CH₃ NCH₃ 2484 Cl 4,5-dihydroisoxazol- CH₃ NCH₃ 4-yl 2485 Cl 3-methyl-4,5-dihydroisoxazol- CH₃ NCH₃ 4-yl 2486 Cl isoxazol-4-yl CH₃ NCH₃ 2487 Cl 3-methylisoxazol-4-yl CH₃ NCH₃ 2488 Cl phenyl CH₃ NCH₃ 2489 Cl benzyl CH₃ NCH₃ 2490 Cl benzoyl CH₃ NCH₃ 2491 Cl 2-pyridyl CH₃ NCH₃ 2492 Cl H Cl NCH₃ 2493 Cl CH₃ Cl NCH₃ 2494 Cl C₂H₅ Cl NCH₃ 2495 Cl n-C₃H₇ Cl NCH₃ 2496 Cl i-C₃H₇ Cl NCH₃ 2497 Cl n-C₄H₉ Cl NCH₃ 2498 Cl i-C₄H₉ Cl NCH₃ 2499 Cl s-C₄H₉ Cl NCH₃ 2500 Cl t-C₄H₉ Cl NCH₃ 2501 Cl CH₂OCH₃ Cl NCH₃ 2502 Cl CF₃ Cl NCH₃ 2503 Cl CF₂H Cl NCH₃ 2504 Cl CN Cl NCH₃ 2505 Cl OH Cl NCH₃ 2506 Cl OCH₃ Cl NCH₃ 2507 Cl NH₂ Cl NCH₃ 2508 Cl NHCH₃ Cl NCH₃ 2509 Cl N(CH₃)₂ Cl NCH₃ 2510 Cl CO₂CH₃ Cl NCH₃ 2511 Cl CO₂C₂H₅ Cl NCH₃ 2512 Cl C(O)CH₃ Cl NCH₃ 2513 Cl C(O)CF₃ Cl NCH₃ 2514 Cl C(═NOCH₃)CH₃ Cl NCH₃ 2515 Cl SO₂CH₃ Cl NCH₃ 2516 Cl SO₂CF₃ Cl NCH₃ 2517 Cl CH₂CO₂H Cl NCH₃ 2518 Cl CH₂COOCH₃ Cl NCH₃ 2519 Cl CH₂COOC₂H₅ Cl NCH₃ 2520 Cl prop-1-en-3-yl Cl NCH₃ 2521 Cl trans-but-2-en-1-yl Cl NCH₃ 2522 Cl cis-but-2-en-1-yl Cl NCH₃ 2523 Cl cis-3-methyl- Cl NCH₃ but-2-en-1-yl 2524 Cl cyclopropyl Cl NCH₃ 2525 Cl cyclopentyl Cl NCH₃ 2526 Cl cyclohexyl Cl NCH₃ 2527 Cl 4,5-dihydroisoxazol- Cl NCH₃ 3-yl 2528 Cl 4-methyl-4,5-dihydroisoxazol- Cl NCH₃ 3-yl 2529 Cl isoxazol-3-yl Cl NCH₃ 2530 Cl 4-methylisoxazol-3-yl Cl NCH₃ 2531 Cl 4,5-dihydroisoxazol- Cl NCH₃ 4-yl 2532 Cl 3-methyl-4,5-dihydroisoxazol- Cl NCH₃ 4-yl 2533 Cl isoxazol-4-yl Cl NCH₃ 2534 Cl 3-methylisoxazol-4-yl Cl NCH₃ 2535 Cl phenyl Cl NCH₃ 2536 Cl benzyl Cl NCH₃ 2537 Cl benzoyl Cl NCH₃ 2538 Cl 2-pyridyl Cl NCH₃ 2539 OCH₃ H H NCH₃ 2540 OCH₃ CH₃ H NCH₃ 2541 OCH₃ C₂H₅ H NCH₃ 2542 OCH₃ n-C₃H₇ H NCH₃ 2543 OCH₃ i-C₃H₇ H NCH₃ 2544 OCH₃ n-C₄H₉ H NCH₃ 2545 OCH₃ i-C₄H₉ H NCH₃ 2546 OCH₃ s-C₄H₉ H NCH₃ 2547 OCH₃ t-C₄H₉ H NCH₃ 2548 OCH₃ CH₂OCH₃ H NCH₃ 2549 OCH₃ CF₃ H NCH₃ 2550 OCH₃ CF₂H H NCH₃ 2551 OCH₃ CN H NCH₃ 2552 OCH₃ OH H NCH₃ 2553 OCH₃ OCH₃ H NCH₃ 2554 OCH₃ NH₂ H NCH₃ 2555 OCH₃ NHCH₃ H NCH₃ 2556 OCH₃ N(CH₃)₂ H NCH₃ 2557 OCH₃ CO₂CH₃ H NCH₃ 2558 OCH₃ CO₂C₂H₅ H NCH₃ 2559 OCH₃ C(O)CH₃ H NCH₃ 2560 OCH₃ C(O)CF₃ H NCH₃ 2561 OCH₃ C(═NOCH₃)CH₃ H NCH₃ 2562 OCH₃ SO₂CH₃ H NCH₃ 2563 OCH₃ SO₂CF₃ H NCH₃ 2564 OCH₃ CH₂CO₂H H NCH₃ 2565 OCH₃ CH₂COOCH₃ H NCH₃ 2566 OCH₃ CH₂COOC₂H₅ H NCH₃ 2567 OCH₃ prop-1-en-3-yl H NCH₃ 2568 OCH₃ trans-but-2-en-1-yl H NCH₃ 2569 OCH₃ cis-but-2-en-1-yl H NCH₃ 2570 OCH₃ cis-3-methyl- H NCH₃ but-2-en-1-yl 2571 OCH₃ cyclopropyl H NCH₃ 2572 OCH₃ cyclopentyl H NCH₃ 2573 OCH₃ cyclohexyl H NCH₃ 2574 OCH₃ 4,5-dihydroisoxazol- H NCH₃ 3-yl 2575 OCH₃ 4-methyl-4,5-dihydroisoxazol- H NCH₃ 3-yl 2576 OCH₃ isoxazol-3-yl H NCH₃ 2577 OCH₃ 4-methylisoxazol-3-yl H NCH₃ 2578 OCH₃ 4,5-dihydroisoxazol- H NCH₃ 4-yl 2579 OCH₃ 3-methyl-4,5-dihydroisoxazol- H NCH₃ 4-yl 2580 OCH₃ isoxazol-4-yl H NCH₃ 2581 OCH₃ 3-methylisoxazol-4-yl H NCH₃ 2582 OCH₃ phenyl H NCH₃ 2583 OCH₃ benzyl H NCH₃ 2584 OCH₃ benzoyl H NCH₃ 2585 OCH₃ 2-pyridyl H NCH₃ 2586 OCH₃ H CH₃ NCH₃ 2587 OCH₃ CH₃ CH₃ NCH₃ 2588 OCH₃ C₂H₅ CH₃ NCH₃ 2589 OCH₃ n-C₃H₇ CH₃ NCH₃ 2590 OCH₃ i-C₃H₇ CH₃ NCH₃ 2591 OCH₃ n-C₄H₉ CH₃ NCH₃ 2592 OCH₃ i-C₄H₉ CH₃ NCH₃ 2593 OCH₃ s-C₄H₉ CH₃ NCH₃ 2594 OCH₃ t-C₄H₉ CH₃ NCH₃ 2595 OCH₃ CH₂OCH₃ CH₃ NCH₃ 2596 OCH₃ CF₃ CH₃ NCH₃ 2597 OCH₃ CF₂H CH₃ NCH₃ 2598 OCH₃ CN CH₃ NCH₃ 2599 OCH₃ OH CH₃ NCH₃ 2600 OCH₃ OCH₃ CH₃ NCH₃ 2601 OCH₃ NH₂ CH₃ NCH₃ 2602 OCH₃ NHCH₃ CH₃ NCH₃ 2603 OCH₃ N(CH₃)₂ CH₃ NCH₃ 2604 OCH₃ CO₂CH₃ CH₃ NCH₃ 2605 OCH₃ CO₂C₂H₅ CH₃ NCH₃ 2606 OCH₃ C(O)CH₃ CH₃ NCH₃ 2607 OCH₃ C(O)CF₃ CH₃ NCH₃ 2608 OCH₃ C(═NOCH₃)CH₃ CH₃ NCH₃ 2609 OCH₃ SO₂CH₃ CH₃ NCH₃ 2610 OCH₃ SO₂CF₃ CH₃ NCH₃ 2611 OCH₃ CH₂CO₂H CH₃ NCH₃ 2612 OCH₃ CH₂COOCH₃ CH₃ NCH₃ 2613 OCH₃ CH₂COOC₂H₅ CH₃ NCH₃ 2614 OCH₃ prop-1-en-3-yl CH₃ NCH₃ 2615 OCH₃ trans-but-2-en-1-yl CH₃ NCH₃ 2616 OCH₃ cis-but-2-en-1-yl CH₃ NCH₃ 2617 OCH₃ cis-3-methyl- CH₃ NCH₃ but-2-en-1-yl 2618 OCH₃ cyclopropyl CH₃ NCH₃ 2619 OCH₃ cyclopentyl CH₃ NCH₃ 2620 OCH₃ cyclohexyl CH₃ NCH₃ 2621 OCH₃ 4,5-dihydroisoxazol- CH₃ NCH₃ 3-yl 2622 OCH₃ 4-methyl-4,5-dihydroisoxazol- CH₃ NCH₃ 3-yl 2623 OCH₃ isoxazol-3-yl CH₃ NCH₃ 2624 OCH₃ 4-methylisoxazol-3-yl CH₃ NCH₃ 2625 OCH₃ 4,5-dihydroisoxazol- CH₃ NCH₃ 4-yl 2626 OCH₃ 3-methyl-4,5-dihydroisoxazol- CH₃ NCH₃ 4-yl 2627 OCH₃ isoxazol-4-yl CH₃ NCH₃ 2628 OCH₃ 3-methylisoxazol-4-yl CH₃ NCH₃ 2629 OCH₃ phenyl CH₃ NCH₃ 2630 OCH₃ benzyl CH₃ NCH₃ 2631 OCH₃ benzoyl CH₃ NCH₃ 2632 OCH₃ 2-pyridyl CH₃ NCH₃ 2633 OCH₃ H Cl NCH₃ 2634 OCH₃ CH₃ Cl NCH₃ 2635 OCH₃ C₂H₅ Cl NCH₃ 2636 OCH₃ n-C₃H₇ Cl NCH₃ 2637 OCH₃ i-C₃H₇ Cl NCH₃ 2638 OCH₃ n-C₄H₉ Cl NCH₃ 2639 OCH₃ i-C₄H₉ Cl NCH₃ 2640 OCH₃ s-C₄H₉ Cl NCH₃ 2641 OCH₃ t-C₄H₉ Cl NCH₃ 2642 OCH₃ CH₂OCH₃ Cl NCH₃ 2643 OCH₃ CF₃ Cl NCH₃ 2644 OCH₃ CF₂H Cl NCH₃ 2645 OCH₃ CN Cl NCH₃ 2646 OCH₃ OH Cl NCH₃ 2647 OCH₃ OCH₃ Cl NCH₃ 2648 OCH₃ NH₂ Cl NCH₃ 2649 OCH₃ NHCH₃ Cl NCH₃ 2650 OCH₃ N(CH₃)₂ Cl NCH₃ 2651 OCH₃ CO₂CH₃ Cl NCH₃ 2652 OCH₃ CO₂C₂H₅ Cl NCH₃ 2653 OCH₃ C(O)CH₃ Cl NCH₃ 2654 OCH₃ C(O)CF₃ Cl NCH₃ 2655 OCH₃ C(═NOCH₃)CH₃ Cl NCH₃ 2656 OCH₃ SO₂CH₃ Cl NCH₃ 2657 OCH₃ SO₂CF₃ Cl NCH₃ 2658 OCH₃ CH₂CO₂H Cl NCH₃ 2659 OCH₃ CH₂COOCH₃ Cl NCH₃ 2660 OCH₃ CH₂COOC₂H₅ Cl NCH₃ 2661 OCH₃ prop-1-en-3-yl Cl NCH₃ 2662 OCH₃ trans-but-2-en-1-yl Cl NCH₃ 2663 OCH₃ cis-but-2-en-1-yl Cl NCH₃ 2664 OCH₃ cis-3-methyl- Cl NCH₃ but-2-en-1-yl 2665 OCH₃ cyclopropyl Cl NCH₃ 2666 OCH₃ cyclopentyl Cl NCH₃ 2667 OCH₃ cyclohexyl Cl NCH₃ 2668 OCH₃ 4,5-dihydroisoxazol- Cl NCH₃ 3-yl 2669 OCH₃ 4-methyl-4,5-dihydroisoxazol- Cl NCH₃ 3-yl 2670 OCH₃ isoxazol-3-yl Cl NCH₃ 2671 OCH₃ 4-methylisoxazol-3-yl Cl NCH₃ 2672 OCH₃ 4,5-dihydroisoxazol- Cl NCH₃ 4-yl 2673 OCH₃ 3-methyl-4,5-dihydroisoxazol- Cl NCH₃ 4-yl 2674 OCH₃ isoxazol-4-yl Cl NCH₃ 2675 OCH₃ 3-methylisoxazol-4-yl Cl NCH₃ 2676 OCH₃ phenyl Cl NCH₃ 2677 OCH₃ benzyl Cl NCH₃ 2678 OCH₃ benzoyl Cl NCH₃ 2679 OCH₃ 2-pyridyl Cl NCH₃ 2680 OCF₃ H H NCH₃ 2681 OCF₃ CH₃ H NCH₃ 2682 OCF₃ C₂H₅ H NCH₃ 2683 OCF₃ n-C₃H₇ H NCH₃ 2684 OCF₃ i-C₃H₇ H NCH₃ 2685 OCF₃ n-C₄H₉ H NCH₃ 2686 OCF₃ i-C₄H₉ H NCH₃ 2687 OCF₃ s-C₄H₉ H NCH₃ 2688 OCF₃ t-C₄H₉ H NCH₃ 2689 OCF₃ CH₂OCH₃ H NCH₃ 2690 OCF₃ CF₃ H NCH₃ 2691 OCF₃ CF₂H H NCH₃ 2692 OCF₃ CN H NCH₃ 2693 OCF₃ OH H NCH₃ 2694 OCF₃ OCH₃ H NCH₃ 2695 OCF₃ NH₂ H NCH₃ 2696 OCF₃ NHCH₃ H NCH₃ 2697 OCF₃ N(CH₃)₂ H NCH₃ 2698 OCF₃ CO₂CH₃ H NCH₃ 2699 OCF₃ CO₂C₂H₅ H NCH₃ 2700 OCF₃ C(O)CH₃ H NCH₃ 2701 OCF₃ C(O)CF₃ H NCH₃ 2702 OCF₃ C(═NOCH₃)CH₃ H NCH₃ 2703 OCF₃ SO₂CH₃ H NCH₃ 2704 OCF₃ SO₂CF₃ H NCH₃ 2705 OCF₃ CH₂CO₂H H NCH₃ 2706 OCF₃ CH₂COOCH₃ H NCH₃ 2707 OCF₃ CH₂COOC₂H₅ H NCH₃ 2708 OCF₃ prop-1-en-3-yl H NCH₃ 2709 OCF₃ trans-but-2-en-1-yl H NCH₃ 2710 OCF₃ cis-but-2-en-1-yl H NCH₃ 2711 OCF₃ cis-3-methyl- H NCH₃ but-2-en-1-yl 2712 OCF₃ cyclopropyl H NCH₃ 2713 OCF₃ cyclopentyl H NCH₃ 2714 OCF₃ cyclohexyl H NCH₃ 2715 OCF₃ 4,5-dihydroisoxazol- H NCH₃ 3-yl 2716 OCF₃ 4-methyl-4,5-dihydroisoxazol- H NCH₃ 3-yl 2717 OCF₃ isoxazol-3-yl H NCH₃ 2718 OCF₃ 4-methylisoxazol-3-yl H NCH₃ 2719 OCF₃ 4,5-dihydroisoxazol- H NCH₃ 4-yl 2720 OCF₃ 3-methyl-4,5-dihydroisoxazol- H NCH₃ 4-yl 2721 OCF₃ isoxazol-4-yl H NCH₃ 2722 OCF₃ 3-methylisoxazol-4-yl H NCH₃ 2723 OCF₃ phenyl H NCH₃ 2724 OCF₃ benzyl H NCH₃ 2725 OCF₃ benzoyl H NCH₃ 2726 OCF₃ 2-pyridyl H NCH₃ 2727 OCF₃ H CH₃ NCH₃ 2728 OCF₃ CH₃ CH₃ NCH₃ 2729 OCF₃ C₂H₅ CH₃ NCH₃ 2730 OCF₃ n-C₃H₇ CH₃ NCH₃ 2731 OCF₃ i-C₃H₇ CH₃ NCH₃ 2732 OCF₃ n-C₄H₉ CH₃ NCH₃ 2733 OCF₃ i-C₄H₉ CH₃ NCH₃ 2734 OCF₃ s-C₄H₉ CH₃ NCH₃ 2735 OCF₃ t-C₄H₉ CH₃ NCH₃ 2736 OCF₃ CH₂OCH₃ CH₃ NCH₃ 2737 OCF₃ CF₃ CH₃ NCH₃ 2738 OCF₃ CF₂H CH₃ NCH₃ 2739 OCF₃ CN CH₃ NCH₃ 2740 OCF₃ OH CH₃ NCH₃ 2741 OCF₃ OCH₃ CH₃ NCH₃ 2742 OCF₃ NH₂ CH₃ NCH₃ 2743 OCF₃ NHCH₃ CH₃ NCH₃ 2744 OCF₃ N(CH₃)₂ CH₃ NCH₃ 2745 OCF₃ CO₂CH₃ CH₃ NCH₃ 2746 OCF₃ CO₂C₂H₅ CH₃ NCH₃ 2747 OCF₃ C(O)CH₃ CH₃ NCH₃ 2748 OCF₃ C(O)CF₃ CH₃ NCH₃ 2749 OCF₃ C(═NOCH₃)CH₃ CH₃ NCH₃ 2750 OCF₃ SO₂CH₃ CH₃ NCH₃ 2751 OCF₃ SO₂CF₃ CH₃ NCH₃ 2752 OCF₃ CH₂CO₂H CH₃ NCH₃ 2753 OCF₃ CH₂COOCH₃ CH₃ NCH₃ 2754 OCF₃ CH₂COOC₂H₅ CH₃ NCH₃ 2755 OCF₃ prop-1-en-3-yl CH₃ NCH₃ 2756 OCF₃ trans-but-2-en-1-yl CH₃ NCH₃ 2757 OCF₃ cis-but-2-en-1-yl CH₃ NCH₃ 2758 OCF₃ cis-3-methyl- CH₃ NCH₃ but-2-en-1-yl 2759 OCF₃ cyclopropyl CH₃ NCH₃ 2760 OCF₃ cyclopentyl CH₃ NCH₃ 2761 OCF₃ cyclohexyl CH₃ NCH₃ 2762 OCF₃ 4,5-dihydroisoxazol- CH₃ NCH₃ 3-yl 2763 OCF₃ 4-methyl-4,5-dihydroisoxazol- CH₃ NCH₃ 3-yl 2764 OCF₃ isoxazol-3-yl CH₃ NCH₃ 2765 OCF₃ 4-methylisoxazol-3-yl CH₃ NCH₃ 2766 OCF₃ 4,5-dihydroisoxazol- CH₃ NCH₃ 4-yl 2767 OCF₃ 3-methyl-4,5-dihydroisoxazol- CH₃ NCH₃ 4-yl 2768 OCF₃ isoxazol-4-yl CH₃ NCH₃ 2769 OCF₃ 3-methylisoxazol-4-yl CH₃ NCH₃ 2770 OCF₃ phenyl CH₃ NCH₃ 2771 OCF₃ benzyl CH₃ NCH₃ 2772 OCF₃ benzoyl CH₃ NCH₃ 2773 OCF₃ 2-pyridyl CH₃ NCH₃ 2774 OCF₃ H Cl NCH₃ 2775 OCF₃ CH₃ Cl NCH₃ 2776 OCF₃ C₂H₅ Cl NCH₃ 2777 OCF₃ n-C₃H₇ Cl NCH₃ 2778 OCF₃ i-C₃H₇ Cl NCH₃ 2779 OCF₃ n-C₄H₉ Cl NCH₃ 2780 OCF₃ i-C₄H₉ Cl NCH₃ 2781 OCF₃ s-C₄H₉ Cl NCH₃ 2782 OCF₃ t-C₄H₉ Cl NCH₃ 2783 OCF₃ CH₂OCH₃ Cl NCH₃ 2784 OCF₃ CF₃ Cl NCH₃ 2785 OCF₃ CF₂H Cl NCH₃ 2786 OCF₃ CN Cl NCH₃ 2787 OCF₃ OH Cl NCH₃ 2788 OCF₃ OCH₃ Cl NCH₃ 2789 OCF₃ NH₂ Cl NCH₃ 2790 OCF₃ NHCH₃ Cl NCH₃ 2791 OCF₃ N(CH₃)₂ Cl NCH₃ 2792 OCF₃ CO₂CH₃ Cl NCH₃ 2793 OCF₃ CO₂C₂H₅ Cl NCH₃ 2794 OCF₃ C(O)CH₃ Cl NCH₃ 2795 OCF₃ C(O)CF₃ Cl NCH₃ 2796 OCF₃ C(═NOCH₃)CH₃ Cl NCH₃ 2797 OCF₃ SO₂CH₃ Cl NCH₃ 2798 OCF₃ SO₂CF₃ Cl NCH₃ 2799 OCF₃ CH₂CO₂H Cl NCH₃ 2800 OCF₃ CH₂COOCH₃ Cl NCH₃ 2801 OCF₃ CH₂COOC₂H₅ Cl NCH₃ 2802 OCF₃ prop-1-en-3-yl Cl NCH₃ 2803 OCF₃ trans-but-2-en-1-yl Cl NCH₃ 2804 OCF₃ cis-but-2-en-1-yl Cl NCH₃ 2805 OCF₃ cis-3-methyl- Cl NCH₃ but-2-en-1-yl 2806 OCF₃ cyclopropyl Cl NCH₃ 2807 OCF₃ cyclopentyl Cl NCH₃ 2808 OCF₃ cyclohexyl Cl NCH₃ 2809 OCF₃ 4,5-dihydroisoxazol- Cl NCH₃ 3-yl 2810 OCF₃ 4-methyl-4,5-dihydroisoxazol- Cl NCH₃ 3-yl 2811 OCF₃ isoxazol-3-yl Cl NCH₃ 2812 OCF₃ 4-methylisoxazol-3-yl Cl NCH₃ 2813 OCF₃ 4,5-dihydroisoxazol- Cl NCH₃ 4-yl 2814 OCF₃ 3-methyl-4,5-dihydroisoxazol- Cl NCH₃ 4-yl 2815 OCF₃ isoxazol-4-yl Cl NCH₃ 2816 OCF₃ 3-methylisoxazol-4-yl Cl NCH₃ 2817 OCF₃ phenyl Cl NCH₃ 2818 OCF₃ benzyl Cl NCH₃ 2819 OCF₃ benzoyl Cl NCH₃ 2820 OCF₃ 2-pyridyl Cl NCH₃ 2821 SCH₃ H H NCH₃ 2822 SCH₃ CH₃ H NCH₃ 2823 SCH₃ C₂H₅ H NCH₃ 2824 SCH₃ n-C₃H₇ H NCH₃ 2825 SCH₃ i-C₃H₇ H NCH₃ 2826 SCH₃ n-C₄H₉ H NCH₃ 2827 SCH₃ i-C₄H₉ H NCH₃ 2828 SCH₃ s-C₄H₉ H NCH₃ 2829 SCH₃ t-C₄H₉ H NCH₃ 2830 SCH₃ CH₂OCH₃ H NCH₃ 2831 SCH₃ CF₃ H NCH₃ 2832 SCH₃ CF₂H H NCH₃ 2833 SCH₃ CN H NCH₃ 2834 SCH₃ OH H NCH₃ 2835 SCH₃ OCH₃ H NCH₃ 2836 SCH₃ NH₂ H NCH₃ 2837 SCH₃ NHCH₃ H NCH₃ 2838 SCH₃ N(CH₃)₂ H NCH₃ 2839 SCH₃ CO₂CH₃ H NCH₃ 2840 SCH₃ CO₂C₂H₅ H NCH₃ 2841 SCH₃ C(O)CH₃ H NCH₃ 2842 SCH₃ C(O)CF₃ H NCH₃ 2843 SCH₃ C(═NOCH₃)CH₃ H NCH₃ 2844 SCH₃ SO₂CH₃ H NCH₃ 2845 SCH₃ SO₂CF₃ H NCH₃ 2846 SCH₃ CH₂CO₂H H NCH₃ 2847 SCH₃ CH₂COOCH₃ H NCH₃ 2848 SCH₃ CH₂COOC₂H₅ H NCH₃ 2849 SCH₃ prop-1-en-3-yl H NCH₃ 2850 SCH₃ trans-but-2-en-1-yl H NCH₃ 2851 SCH₃ cis-but-2-en-1-yl H NCH₃ 2852 SCH₃ cis-3-methyl- H NCH₃ but-2-en-1-yl 2853 SCH₃ cyclopropyl H NCH₃ 2854 SCH₃ cyclopentyl H NCH₃ 2855 SCH₃ cyclohexyl H NCH₃ 2856 SCH₃ 4,5-dihydroisoxazol- H NCH₃ 3-yl 2857 SCH₃ 4-methyl-4,5-dihydroisoxazol- H NCH₃ 3-yl 2858 SCH₃ isoxazol-3-yl H NCH₃ 2859 SCH₃ 4-methylisoxazol-3-yl H NCH₃ 2860 SCH₃ 4,5-dihydroisoxazol- H NCH₃ 4-yl 2861 SCH₃ 3-methyl-4,5-dihydroisoxazol- H NCH₃ 4-yl 2862 SCH₃ isoxazol-4-yl H NCH₃ 2863 SCH₃ 3-methylisoxazol-4-yl H NCH₃ 2864 SCH₃ phenyl H NCH₃ 2865 SCH₃ benzyl H NCH₃ 2866 SCH₃ benzoyl H NCH₃ 2867 SCH₃ 2-pyridyl H NCH₃ 2868 SCH₃ H CH₃ NCH₃ 2869 SCH₃ CH₃ CH₃ NCH₃ 2870 SCH₃ C₂H₅ CH₃ NCH₃ 2871 SCH₃ n-C₃H₇ CH₃ NCH₃ 2872 SCH₃ i-C₃H₇ CH₃ NCH₃ 2873 SCH₃ n-C₄H₉ CH₃ NCH₃ 2874 SCH₃ i-C₄H₉ CH₃ NCH₃ 2875 SCH₃ s-C₄H₉ CH₃ NCH₃ 2876 SCH₃ t-C₄H₉ CH₃ NCH₃ 2877 SCH₃ CH₂OCH₃ CH₃ NCH₃ 2878 SCH₃ CF₃ CH₃ NCH₃ 2879 SCH₃ CF₂H CH₃ NCH₃ 2880 SCH₃ CN CH₃ NCH₃ 2881 SCH₃ OH CH₃ NCH₃ 2882 SCH₃ OCH₃ CH₃ NCH₃ 2883 SCH₃ NH₂ CH₃ NCH₃ 2884 SCH₃ NHCH₃ CH₃ NCH₃ 2885 SCH₃ N(CH₃)₂ CH₃ NCH₃ 2886 SCH₃ CO₂CH₃ CH₃ NCH₃ 2887 SCH₃ CO₂C₂H₅ CH₃ NCH₃ 2888 SCH₃ C(O)CH₃ CH₃ NCH₃ 2889 SCH₃ C(O)CF₃ CH₃ NCH₃ 2890 SCH₃ C(═NOCH₃)CH₃ CH₃ NCH₃ 2891 SCH₃ SO₂CH₃ CH₃ NCH₃ 2892 SCH₃ SO₂CF₃ CH₃ NCH₃ 2893 SCH₃ CH₂CO₂H CH₃ NCH₃ 2894 SCH₃ CH₂COOCH₃ CH₃ NCH₃ 2895 SCH₃ CH₂COOC₂H₅ CH₃ NCH₃ 2896 SCH₃ prop-1-en-3-yl CH₃ NCH₃ 2897 SCH₃ trans-but-2-en-1-yl CH₃ NCH₃ 2898 SCH₃ cis-but-2-en-1-yl CH₃ NCH₃ 2899 SCH₃ cis-3-methyl- CH₃ NCH₃ but-2-en-1-yl 2900 SCH₃ cyclopropyl CH₃ NCH₃ 2901 SCH₃ cyclopentyl CH₃ NCH₃ 2902 SCH₃ cyclohexyl CH₃ NCH₃ 2903 SCH₃ 4,5-dihydroisoxazol- CH₃ NCH₃ 3-yl 2904 SCH₃ 4-methyl-4,5-dihydroisoxazol- CH₃ NCH₃ 3-yl 2905 SCH₃ isoxazol-3-yl CH₃ NCH₃ 2906 SCH₃ 4-methylisoxazol-3-yl CH₃ NCH₃ 2907 SCH₃ 4,5-dihydroisoxazol- CH₃ NCH₃ 4-yl 2908 SCH₃ 3-methyl-4,5-dihydroisoxazol- CH₃ NCH₃ 4-yl 2909 SCH₃ isoxazol-4-yl CH₃ NCH₃ 2910 SCH₃ 3-methylisoxazol-4-yl CH₃ NCH₃ 2911 SCH₃ phenyl CH₃ NCH₃ 2912 SCH₃ benzyl CH₃ NCH₃ 2913 SCH₃ benzoyl CH₃ NCH₃ 2914 SCH₃ 2-pyridyl CH₃ NCH₃ 2915 SCH₃ H Cl NCH₃ 2916 SCH₃ CH₃ Cl NCH₃ 2917 SCH₃ C₂H₅ Cl NCH₃ 2918 SCH₃ n-C₃H₇ Cl NCH₃ 2919 SCH₃ i-C₃H₇ Cl NCH₃ 2920 SCH₃ n-C₄H₉ Cl NCH₃ 2921 SCH₃ i-C₄H₉ Cl NCH₃ 2922 SCH₃ s-C₄H₉ Cl NCH₃ 2923 SCH₃ t-C₄H₉ Cl NCH₃ 2924 SCH₃ CH₂OCH₃ Cl NCH₃ 2925 SCH₃ CF₃ Cl NCH₃ 2926 SCH₃ CF₂H Cl NCH₃ 2927 SCH₃ CN Cl NCH₃ 2928 SCH₃ OH Cl NCH₃ 2929 SCH₃ OCH₃ Cl NCH₃ 2930 SCH₃ NH₂ Cl NCH₃ 2931 SCH₃ NHCH₃ Cl NCH₃ 2932 SCH₃ N(CH₃)₂ Cl NCH₃ 2933 SCH₃ CO₂CH₃ Cl NCH₃ 2934 SCH₃ CO₂C₂H₅ Cl NCH₃ 2935 SCH₃ C(O)CH₃ Cl NCH₃ 2936 SCH₃ C(O)CF₃ Cl NCH₃ 2937 SCH₃ C(═NOCH₃)CH₃ Cl NCH₃ 2938 SCH₃ SO₂CH₃ Cl NCH₃ 2939 SCH₃ SO₂CF₃ Cl NCH₃ 2940 SCH₃ CH₂CO₂H Cl NCH₃ 2941 SCH₃ CH₂COOCH₃ Cl NCH₃ 2942 SCH₃ CH₂COOC₂H₅ Cl NCH₃ 2943 SCH₃ prop-1-en-3-yl Cl NCH₃ 2944 SCH₃ trans-but-2-en-1-yl Cl NCH₃ 2945 SCH₃ cis-but-2-en-1-yl Cl NCH₃ 2946 SCH₃ cis-3-methyl- Cl NCH₃ but-2-en-1-yl 2947 SCH₃ cyclopropyl Cl NCH₃ 2948 SCH₃ cyclopentyl Cl NCH₃ 2949 SCH₃ cyclohexyl Cl NCH₃ 2950 SCH₃ 4,5-dihydroisoxazol- Cl NCH₃ 3-yl 2951 SCH₃ 4-methyl-4,5-dihydroisoxazol- Cl NCH₃ 3-yl 2952 SCH₃ isoxazol-3-yl Cl NCH₃ 2953 SCH₃ 4-methylisoxazol-3-yl Cl NCH₃ 2954 SCH₃ 4,5-dihydroisoxazol- Cl NCH₃ 4-yl 2955 SCH₃ 3-methyl-4,5-dihydroisoxazol- Cl NCH₃ 4-yl 2956 SCH₃ isoxazol-4-yl Cl NCH₃ 2957 SCH₃ 3-methylisoxazol-4-yl Cl NCH₃ 2958 SCH₃ phenyl Cl NCH₃ 2959 SCH₃ benzyl Cl NCH₃ 2960 SCH₃ benzoyl Cl NCH₃ 2961 SCH₃ 2-pyridyl Cl NCH₃ 2962 SO₂CH₃ H H NCH₃ 2963 SO₂CH₃ CH₃ H NCH₃ 2964 SO₂CH₃ C₂H₅ H NCH₃ 2965 SO₂CH₃ n-C₃H₇ H NCH₃ 2966 SO₂CH₃ i-C₃H₇ H NCH₃ 2967 SO₂CH₃ n-C₄H₉ H NCH₃ 2968 SO₂CH₃ i-C₄H₉ H NCH₃ 2969 SO₂CH₃ s-C₄H₉ H NCH₃ 2970 SO₂CH₃ t-C₄H₉ H NCH₃ 2971 SO₂CH₃ CH₂OCH₃ H NCH₃ 2972 SO₂CH₃ CF₃ H NCH₃ 2973 SO₂CH₃ CF₂H H NCH₃ 2974 SO₂CH₃ CN H NCH₃ 2975 SO₂CH₃ OH H NCH₃ 2976 SO₂CH₃ OCH₃ H NCH₃ 2977 SO₂CH₃ NH₂ H NCH₃ 2978 SO₂CH₃ NHCH₃ H NCH₃ 2979 SO₂CH₃ N(CH₃)₂ H NCH₃ 2980 SO₂CH₃ CO₂CH₃ H NCH₃ 2981 SO₂CH₃ CO₂C₂H₅ H NCH₃ 2982 SO₂CH₃ C(O)CH₃ H NCH₃ 2983 SO₂CH₃ C(O)CF₃ H NCH₃ 2984 SO₂CH₃ C(═NOCH₃)CH₃ H NCH₃ 2985 SO₂CH₃ SO₂CH₃ H NCH₃ 2986 SO₂CH₃ SO₂CF₃ H NCH₃ 2987 SO₂CH₃ CH₂CO₂H H NCH₃ 2988 SO₂CH₃ CH₂COOCH₃ H NCH₃ 2989 SO₂CH₃ CH₂COOC₂H₅ H NCH₃ 2990 SO₂CH₃ prop-1-en-3-yl H NCH₃ 2991 SO₂CH₃ trans-but-2-en-1-yl H NCH₃ 2992 SO₂CH₃ cis-but-2-en-1-yl H NCH₃ 2993 SO₂CH₃ cis-3-methyl- H NCH₃ but-2-en-1-yl 2994 SO₂CH₃ cyclopropyl H NCH₃ 2995 SO₂CH₃ cyclopentyl H NCH₃ 2996 SO₂CH₃ cyclohexyl H NCH₃ 2997 SO₂CH₃ 4,5-dihydroisoxazol- H NCH₃ 3-yl 2998 SO₂CH₃ 4-methyl-4,5-dihydroisoxazol- H NCH₃ 3-yl 2999 SO₂CH₃ isoxazol-3-yl H NCH₃ 3000 SO₂CH₃ 4-methylisoxazol-3-yl H NCH₃ 3001 SO₂CH₃ 4,5-dihydroisoxazol- H NCH₃ 4-yl 3002 SO₂CH₃ 3-methyl-4,5-dihydroisoxazol- H NCH₃ 4-yl 3003 SO₂CH₃ isoxazol-4-yl H NCH₃ 3004 SO₂CH₃ 3-methylisoxazol-4-yl H NCH₃ 3005 SO₂CH₃ phenyl H NCH₃ 3006 SO₂CH₃ benzyl H NCH₃ 3007 SO₂CH₃ benzoyl H NCH₃ 3008 SO₂CH₃ 2-pyridyl H NCH₃ 3009 SO₂CH₃ H CH₃ NCH₃ 3010 SO₂CH₃ CH₃ CH₃ NCH₃ 3011 SO₂CH₃ C₂H₅ CH₃ NCH₃ 3012 SO₂CH₃ n-C₃H₇ CH₃ NCH₃ 3013 SO₂CH₃ i-C₃H₇ CH₃ NCH₃ 3014 SO₂CH₃ n-C₄H₉ CH₃ NCH₃ 3015 SO₂CH₃ i-C₄H₉ CH₃ NCH₃ 3016 SO₂CH₃ s-C₄H₉ CH₃ NCH₃ 3017 SO₂CH₃ t-C₄H₉ CH₃ NCH₃ 3018 SO₂CH₃ CH₂OCH₃ CH₃ NCH₃ 3019 SO₂CH₃ CF₃ CH₃ NCH₃ 3020 SO₂CH₃ CF₂H CH₃ NCH₃ 3021 SO₂CH₃ CN CH₃ NCH₃ 3022 SO₂CH₃ OH CH₃ NCH₃ 3023 SO₂CH₃ OCH₃ CH₃ NCH₃ 3024 SO₂CH₃ NH₂ CH₃ NCH₃ 3025 SO₂CH₃ NHCH₃ CH₃ NCH₃ 3026 SO₂CH₃ N(CH₃)₂ CH₃ NCH₃ 3027 SO₂CH₃ CO₂CH₃ CH₃ NCH₃ 3028 SO₂CH₃ CO₂C₂H₅ CH₃ NCH₃ 3029 SO₂CH₃ C(O)CH₃ CH₃ NCH₃ 3030 SO₂CH₃ C(O)CF₃ CH₃ NCH₃ 3031 SO₂CH₃ C(═NOCH₃)CH₃ CH₃ NCH₃ 3032 SO₂CH₃ SO₂CH₃ CH₃ NCH₃ 3033 SO₂CH₃ SO₂CF₃ CH₃ NCH₃ 3034 SO₂CH₃ CH₂CO₂H CH₃ NCH₃ 3035 SO₂CH₃ CH₂COOCH₃ CH₃ NCH₃ 3036 SO₂CH₃ CH₂COOC₂H₅ CH₃ NCH₃ 3037 SO₂CH₃ prop-1-en-3-yl CH₃ NCH₃ 3038 SO₂CH₃ trans-but-2-en-1-yl CH₃ NCH₃ 3039 SO₂CH₃ cis-but-2-en-1-yl CH₃ NCH₃ 3040 SO₂CH₃ cis-3-methyl- CH₃ NCH₃ but-2-en-1-yl 3041 SO₂CH₃ cyclopropyl CH₃ NCH₃ 3042 SO₂CH₃ cyclopentyl CH₃ NCH₃ 3043 SO₂CH₃ cyclohexyl CH₃ NCH₃ 3044 SO₂CH₃ 4,5-dihydroisoxazol- CH₃ NCH₃ 3-yl 3045 SO₂CH₃ 4-methyl-4,5-dihydroisoxazol- CH₃ NCH₃ 3-yl 3046 SO₂CH₃ isoxazol-3-yl CH₃ NCH₃ 3047 SO₂CH₃ 4-methylisoxazol-3-yl CH₃ NCH₃ 3048 SO₂CH₃ 4,5-dihydroisoxazol- CH₃ NCH₃ 4-yl 3049 SO₂CH₃ 3-methyl-4,5-dihydroisoxazol- CH₃ NCH₃ isoxazol-4-yl 3050 SO₂CH₃ isoxazol-4-yl CH₃ NCH₃ 3051 SO₂CH₃ 3-methylisoxazol-4-yl CH₃ NCH₃ 3052 SO₂CH₃ phenyl CH₃ NCH₃ 3053 SO₂CH₃ benzyl CH₃ NCH₃ 3054 SO₂CH₃ benzoyl CH₃ NCH₃ 3055 SO₂CH₃ 2-pyridyl CH₃ NCH₃ 3056 SO₂CH₃ H Cl NCH₃ 3057 SO₂CH₃ CH₃ Cl NCH₃ 3058 SO₂CH₃ C₂H₅ Cl NCH₃ 3059 SO₂CH₃ n-C₃H₇ Cl NCH₃ 3060 SO₂CH₃ i-C₃H₇ Cl NCH₃ 3061 SO₂CH₃ n-C₄H₉ Cl NCH₃ 3062 SO₂CH₃ i-C₄H₉ Cl NCH₃ 3063 SO₂CH₃ s-C₄H₉ Cl NCH₃ 3064 SO₂CH₃ t-C₄H₉ Cl NCH₃ 3065 SO₂CH₃ CH₂OCH₃ Cl NCH₃ 3066 SO₂CH₃ CF₃ Cl NCH₃ 3067 SO₂CH₃ CF₂H Cl NCH₃ 3068 SO₂CH₃ CN Cl NCH₃ 3069 SO₂CH₃ OH Cl NCH₃ 3070 SO₂CH₃ OCH₃ Cl NCH₃ 3071 SO₂CH₃ NH₂ Cl NCH₃ 3072 SO₂CH₃ NHCH₃ Cl NCH₃ 3073 SO₂CH₃ N(CH₃)₂ Cl NCH₃ 3074 SO₂CH₃ CO₂CH₃ Cl NCH₃ 3075 SO₂CH₃ CO₂C₂H₅ Cl NCH₃ 3076 SO₂CH₃ C(O)CH₃ Cl NCH₃ 3077 SO₂CH₃ C(O)CF₃ Cl NCH₃ 3078 SO₂CH₃ C(═NOCH₃)CH₃ Cl NCH₃ 3079 SO₂CH₃ SO₂CH₃ Cl NCH₃ 3080 SO₂CH₃ SO₂CF₃ Cl NCH₃ 3081 SO₂CH₃ CH₂CO₂H Cl NCH₃ 3082 SO₂CH₃ CH₂COOCH₃ Cl NCH₃ 3083 SO₂CH₃ CH₂COOC₂H₅ Cl NCH₃ 3084 SO₂CH₃ prop-1-en-3-yl Cl NCH₃ 3085 SO₂CH₃ trans-but-2-en-1-yl Cl NCH₃ 3086 SO₂CH₃ cis-but-2-en-1-yl Cl NCH₃ 3087 SO₂CH₃ cis-3-methyl- Cl NCH₃ but-2-en-1-yl 3088 SO₂CH₃ cyclopropyl Cl NCH₃ 3089 SO₂CH₃ cyclopentyl Cl NCH₃ 3090 SO₂CH₃ cyclohexyl Cl NCH₃ 3091 SO₂CH₃ 4,5-dihydroisoxazol- Cl NCH₃ 3-yl 3092 SO₂CH₃ 4-methyl-4,5-dihydroisoxazol- Cl NCH₃ 3-yl 3093 SO₂CH₃ isoxazol-3-yl Cl NCH₃ 3094 SO₂CH₃ 4-methylisoxazol-3-yl Cl NCH₃ 3095 SO₂CH₃ 4,5-dihydroisoxazol- Cl NCH₃ 4-yl 3096 SO₂CH₃ 3-methyl-4,5-dihydroisoxazol- Cl NCH₃ 4-yl 3097 SO₂CH₃ isoxazol-4-yl Cl NCH₃ 3098 SO₂CH₃ 3-methylisoxazol-4-yl Cl NCH₃ 3099 SO₂CH₃ phenyl Cl NCH₃ 3100 SO₂CH₃ benzyl Cl NCH₃ 3101 SO₂CH₃ benzoyl Cl NCH₃ 3102 SO₂CH₃ 2-pyridyl Cl NCH₃ 3103 CF₃ H H NCH₃ 3104 CF₃ CH₃ H NCH₃ 3105 CF₃ C₂H₅ H NCH₃ 3106 CF₃ n-C₃H₇ H NCH₃ 3107 CF₃ i-C₃H₇ H NCH₃ 3108 CF₃ n-C₄H₉ H NCH₃ 3109 CF₃ i-C₄H₉ H NCH₃ 3110 CF₃ s-C₄H₉ H NCH₃ 3111 CF₃ t-C₄H₉ H NCH₃ 3112 CF₃ CH₂OCH₃ H NCH₃ 3113 CF₃ CF₃ H NCH₃ 3114 CF₃ CF₂H H NCH₃ 3115 CF₃ CN H NCH₃ 3116 CF₃ OH H NCH₃ 3117 CF₃ OCH₃ H NCH₃ 3118 CF₃ NH₂ H NCH₃ 3119 CF₃ NHCH₃ H NCH₃ 3120 CF₃ N(CH₃)₂ H NCH₃ 3121 CF₃ CO₂CH₃ H NCH₃ 3122 CF₃ CO₂C₂H₅ H NCH₃ 3123 CF₃ C(O)CH₃ H NCH₃ 3124 CF₃ C(O)CF₃ H NCH₃ 3125 CF₃ C(═NOCH₃)CH₃ H NCH₃ 3126 CF₃ SO₂CH₃ H NCH₃ 3127 CF₃ SO₂CF₃ H NCH₃ 3128 CF₃ CH₂CO₂H H NCH₃ 3129 CF₃ CH₂COOCH₃ H NCH₃ 3130 CF₃ CH₂COOC₂H₅ H NCH₃ 3131 CF₃ prop-1-en-3-yl H NCH₃ 3132 CF₃ trans-but-2-en-1-yl H NCH₃ 3133 CF₃ cis-but-2-en-1-yl H NCH₃ 3134 CF₃ cis-3-methyl- H NCH₃ but-2-en-1-yl 3135 CF₃ cyclopropyl H NCH₃ 3136 CF₃ cyclopentyl H NCH₃ 3137 CF₃ cyclohexyl H NCH₃ 3138 CF₃ 4,5-dihydroisoxazol- H NCH₃ 3-yl 3139 CF₃ 4-methyl-4,5-dihydroisoxazol- H NCH₃ 3-yl 3140 CF₃ isoxazol-3-yl H NCH₃ 3141 CF₃ 4-methylisoxazol-3-yl H NCH₃ 3142 CF₃ 4,5-dihydroisoxazol- H NCH₃ 4-yl 3143 CF₃ 3-methyl-4,5-dihydroisoxazol- H NCH₃ 4-yl 3144 CF₃ isoxazol-4-yl H NCH₃ 3145 CF₃ 3-methylisoxazol-4-yl H NCH₃ 3146 CF₃ phenyl H NCH₃ 3147 CF₃ benzyl H NCH₃ 3148 CF₃ benzoyl H NCH₃ 3149 CF₃ 2-pyridyl H NCH₃ 3150 CF₃ H CH₃ NCH₃ 3151 CF₃ CH₃ CH₃ NCH₃ 3152 CF₃ C₂H₅ CH₃ NCH₃ 3153 CF₃ n-C₃H₇ CH₃ NCH₃ 3154 CF₃ i-C₃H₇ CH₃ NCH₃ 3155 CF₃ n-C₄H₉ CH₃ NCH₃ 3156 CF₃ i-C₄H₉ CH₃ NCH₃ 3157 CF₃ s-C₄H₉ CH₃ NCH₃ 3158 CF₃ t-C₄H₉ CH₃ NCH₃ 3159 CF₃ CH₂OCH₃ CH₃ NCH₃ 3160 CF₃ CF₃ CH₃ NCH₃ 3161 CF₃ CF₂H CH₃ NCH₃ 3162 CF₃ CN CH₃ NCH₃ 3163 CF₃ OH CH₃ NCH₃ 3164 CF₃ OCH₃ CH₃ NCH₃ 3165 CF₃ NH₂ CH₃ NCH₃ 3166 CF₃ NHCH₃ CH₃ NCH₃ 3167 CF₃ N(CH₃)₂ CH₃ NCH₃ 3168 CF₃ CO₂CH₃ CH₃ NCH₃ 3169 CF₃ CO₂C₂H₅ CH₃ NCH₃ 3170 CF₃ C(O)CH₃ CH₃ NCH₃ 3171 CF₃ C(O)CF₃ CH₃ NCH₃ 3172 CF₃ C(═NOCH₃)CH₃ CH₃ NCH₃ 3173 CF₃ SO₂CH₃ CH₃ NCH₃ 3174 CF₃ SO₂CF₃ CH₃ NCH₃ 3175 CF₃ CH₂CO₂H CH₃ NCH₃ 3176 CF₃ CH₂COOCH₃ CH₃ NCH₃ 3177 CF₃ CH₂COOC₂H₅ CH₃ NCH₃ 3178 CF₃ prop-1-en-3-yl CH₃ NCH₃ 3179 CF₃ trans-but-2-en-1-yl CH₃ NCH₃ 3180 CF₃ cis-but-2-en-1-yl CH₃ NCH₃ 3181 CF₃ cis-3-methyl- CH₃ NCH₃ but-2-en-1-yl 3182 CF₃ cyclopropyl CH₃ NCH₃ 3183 CF₃ cyclopentyl CH₃ NCH₃ 3184 CF₃ cyclohexyl CH₃ NCH₃ 3185 CF₃ 4,5-dihydroisoxazol- CH₃ NCH₃ 3-yl 3186 CF₃ 4-methyl-4,5-dihydroisoxazol- CH₃ NCH₃ 3-yl 3187 CF₃ isoxazol-3-yl CH₃ NCH₃ 3188 CF₃ 4-methylisoxazol-3-yl CH₃ NCH₃ 3189 CF₃ 4,5-dihydroisoxazol- CH₃ NCH₃ 4-yl 3190 CF₃ 3-methyl-4,5-dihydroisoxazol- CH₃ NCH₃ 4-yl 3191 CF₃ isoxazol-4-yl CH₃ NCH₃ 3192 CF₃ 3-methylisoxazol-4-yl CH₃ NCH₃ 3193 CF₃ phenyl CH₃ NCH₃ 3194 CF₃ benzyl CH₃ NCH₃ 3195 CF₃ benzoyl CH₃ NCH₃ 3196 CF₃ 2-pyridyl CH₃ NCH₃ 3197 CF₃ H Cl NCH₃ 3198 CF₃ CH₃ Cl NCH₃ 3199 CF₃ C₂H₅ Cl NCH₃ 3200 CF₃ n-C₃H₇ Cl NCH₃ 3201 CF₃ i-C₃H₇ Cl NCH₃ 3202 CF₃ n-C₄H₉ Cl NCH₃ 3203 CF₃ i-C₄H₉ Cl NCH₃ 3204 CF₃ s-C₄H₉ Cl NCH₃ 3205 CF₃ t-C₄H₉ Cl NCH₃ 3206 CF₃ CH₂OCH₃ Cl NCH₃ 3207 CF₃ CF₃ Cl NCH₃ 3208 CF₃ CF₂H Cl NCH₃ 3209 CF₃ CN Cl NCH₃ 3210 CF₃ OH Cl NCH₃ 3211 CF₃ OCH₃ Cl NCH₃ 3212 CF₃ NH₂ Cl NCH₃ 3213 CF₃ NHCH₃ Cl NCH₃ 3214 CF₃ N(CH₃)₂ Cl NCH₃ 3215 CF₃ CO₂CH₃ Cl NCH₃ 3216 CF₃ CO₂C₂H₅ Cl NCH₃ 3217 CF₃ C(O)CH₃ Cl NCH₃ 3218 CF₃ C(O)CF₃ Cl NCH₃ 3219 CF₃ C(═NOCH₃)CH₃ Cl NCH₃ 3220 CF₃ SO₂CH₃ Cl NCH₃ 3221 CF₃ SO₂CF₃ Cl NCH₃ 3222 CF₃ CH₂CO₂H Cl NCH₃ 3223 CF₃ CH₂COOCH₃ Cl NCH₃ 3224 CF₃ CH₂COOC₂H₅ Cl NCH₃ 3225 CF₃ prop-1-en-3-yl Cl NCH₃ 3226 CF₃ trans-but-2-en-1-yl Cl NCH₃ 3227 CF₃ cis-but-2-en-1-yl Cl NCH₃ 3228 CF₃ cis-3-methyl- Cl NCH₃ but-2-en-1-yl 3229 CF₃ cyclopropyl Cl NCH₃ 3230 CF₃ cyclopentyl Cl NCH₃ 3231 CF₃ cyclohexyl Cl NCH₃ 3232 CF₃ 4,5-dihydroisoxazol- Cl NCH₃ 3-yl 3233 CF₃ 4-methyl-4,5-dihydroisoxazol- Cl NCH₃ 3-yl 3234 CF₃ isoxazol-3-yl Cl NCH₃ 3235 CF₃ 4-methylisoxazol-3-yl Cl NCH₃ 3236 CF₃ 4,5-dihydroisoxazol- Cl NCH₃ 4-yl 3237 CF₃ 3-methyl-4,5-dihydroisoxazol- Cl NCH₃ 4-yl 3238 CF₃ isoxazol-4-yl Cl NCH₃ 3239 CF₃ 3-methylisoxazol-4-yl Cl NCH₃ 3240 CF₃ phenyl Cl NCH₃ 3241 CF₃ benzyl Cl NCH₃ 3242 CF₃ benzoyl Cl NCH₃ 3243 CF₃ 2-pyridyl Cl NCH₃ 3244 C₂H₅ H H NCH₃ 3245 C₂H₅ CH₃ H NCH₃ 3246 C₂H₅ C₂H₅ H NCH₃ 3247 C₂H₅ n-C₃H₇ H NCH₃ 3248 C₂H₅ i-C₃H₇ H NCH₃ 3249 C₂H₅ n-C₄H₉ H NCH₃ 3250 C₂H₅ i-C₄H₉ H NCH₃ 3251 C₂H₅ s-C₄H₉ H NCH₃ 3252 C₂H₅ t-C₄H₉ H NCH₃ 3253 C₂H₅ CH₂OCH₃ H NCH₃ 3254 C₂H₅ CF₃ H NCH₃ 3255 C₂H₅ CF₂H H NCH₃ 3256 C₂H₅ CN H NCH₃ 3257 C₂H₅ OH H NCH₃ 3258 C₂H₅ OCH₃ H NCH₃ 3259 C₂H₅ NH₂ H NCH₃ 3260 C₂H₅ NHCH₃ H NCH₃ 3261 C₂H₅ N(CH₃)₂ H NCH₃ 3262 C₂H₅ CO₂CH₃ H NCH₃ 3263 C₂H₅ CO₂C₂H₅ H NCH₃ 3264 C₂H₅ C(O)CH₃ H NCH₃ 3265 C₂H₅ C(O)CF₃ H NCH₃ 3266 C₂H₅ C(═NOCH₃)CH₃ H NCH₃ 3267 C₂H₅ SO₂CH₃ H NCH₃ 3268 C₂H₅ SO₂CF₃ H NCH₃ 3269 C₂H₅ CH₂CO₂H H NCH₃ 3270 C₂H₅ CH₂COOCH₃ H NCH₃ 3271 C₂H₅ CH₂COOC₂H₅ H NCH₃ 3272 C₂H₅ prop-1-en-3-yl H NCH₃ 3273 C₂H₅ trans-but-2-en-1-yl H NCH₃ 3274 C₂H₅ cis-but-2-en-1-yl H NCH₃ 3275 C₂H₅ cis-3-methyl- H NCH₃ but-2-en-1-yl 3276 C₂H₅ cyclopropyl H NCH₃ 3277 C₂H₅ cyclopentyl H NCH₃ 3278 C₂H₅ cyclohexyl H NCH₃ 3279 C₂H₅ 4,5-dihydroisoxazol- H NCH₃ 3-yl 3280 C₂H₅ 4-methyl-4,5-dihydroisoxazol- H NCH₃ 3-yl 3281 C₂H₅ isoxazol-3-yl H NCH₃ 3282 C₂H₅ 4-methylisoxazol-3-yl H NCH₃ 3283 C₂H₅ 4,5-dihydroisoxazol- H NCH₃ 4-yl 3284 C₂H₅ 3-methyl-4,5-dihydroisoxazol- H NCH₃ 4-yl 3285 C₂H₅ isoxazol-4-yl H NCH₃ 3286 C₂H₅ 3-methylisoxazol-4-yl H NCH₃ 3287 C₂H₅ phenyl H NCH₃ 3288 C₂H₅ benzyl H NCH₃ 3289 C₂H₅ benzoyl H NCH₃ 3290 C₂H₅ 2-pyridyl H NCH₃ 3291 C₂H₅ H CH₃ NCH₃ 3292 C₂H₅ CH₃ CH₃ NCH₃ 3293 C₂H₅ C₂H₅ CH₃ NCH₃ 3294 C₂H₅ n-C₃H₇ CH₃ NCH₃ 3295 C₂H₅ i-C₃H₇ CH₃ NCH₃ 3296 C₂H₅ n-C₄H₉ CH₃ NCH₃ 3297 C₂H₅ i-C₄H₉ CH₃ NCH₃ 3298 C₂H₅ s-C₄H₉ CH₃ NCH₃ 3299 C₂H₅ t-C₄H₉ CH₃ NCH₃ 3300 C₂H₅ CH₂OCH₃ CH₃ NCH₃ 3301 C₂H₅ CF₃ CH₃ NCH₃ 3302 C₂H₅ CF₂H CH₃ NCH₃ 3303 C₂H₅ CN CH₃ NCH₃ 3304 C₂H₅ OH CH₃ NCH₃ 3305 C₂H₅ OCH₃ CH₃ NCH₃ 3306 C₂H₅ NH₂ CH₃ NCH₃ 3307 C₂H₅ NHCH₃ CH₃ NCH₃ 3308 C₂H₅ N(CH₃)₂ CH₃ NCH₃ 3309 C₂H₅ CO₂CH₃ CH₃ NCH₃ 3310 C₂H₅ CO₂C₂H₅ CH₃ NCH₃ 3311 C₂H₅ C(O)CH₃ CH₃ NCH₃ 3312 C₂H₅ C(O)CF₃ CH₃ NCH₃ 3313 C₂H₅ C(═NOCH₃)CH₃ CH₃ NCH₃ 3314 C₂H₅ SO₂CH₃ CH₃ NCH₃ 3315 C₂H₅ SO₂CF₃ CH₃ NCH₃ 3316 C₂H₅ CH₂CO₂H CH₃ NCH₃ 3317 C₂H₅ CH₂COOCH₃ CH₃ NCH₃ 3318 C₂H₅ CH₂COOC₂H₅ CH₃ NCH₃ 3319 C₂H₅ prop-1-en-3-yl CH₃ NCH₃ 3320 C₂H₅ trans-but-2-en-1-yl CH₃ NCH₃ 3321 C₂H₅ cis-but-2-en-1-yl CH₃ NCH₃ 3322 C₂H₅ cis-3-methyl- CH₃ NCH₃ but-2-en-1-yl 3323 C₂H₅ cyclopropyl CH₃ NCH₃ 3324 C₂H₅ cyclopentyl CH₃ NCH₃ 3325 C₂H₅ cyclohexyl CH₃ NCH₃ 3326 C₂H₅ 4,5-dihydroisoxazol- CH₃ NCH₃ 3-yl 3327 C₂H₅ 4-methyl-4,5-dihydroisoxazol- CH₃ NCH₃ 3-yl 3328 C₂H₅ isoxazol-3-yl CH₃ NCH₃ 3329 C₂H₅ 4-methylisoxazol-3-yl CH₃ NCH₃ 3330 C₂H₅ 4,5-dihydroisoxazol- CH₃ NCH₃ 4-yl 3331 C₂H₅ 3-methyl-4,5-dihydroisoxazol- CH₃ NCH₃ 4-yl 3332 C₂H₅ isoxazol-4-yl CH₃ NCH₃ 3333 C₂H₅ 3-methylisoxazol-4-yl CH₃ NCH₃ 3334 C₂H₅ phenyl CH₃ NCH₃ 3335 C₂H₅ benzyl CH₃ NCH₃ 3336 C₂H₅ benzoyl CH₃ NCH₃ 3337 C₂H₅ 2-pyridyl CH₃ NCH₃ 3338 C₂H₅ H Cl NCH₃ 3339 C₂H₅ CH₃ Cl NCH₃ 3340 C₂H₅ C₂H₅ Cl NCH₃ 3341 C₂H₅ n-C₃H₇ Cl NCH₃ 3342 C₂H₅ i-C₃H₇ Cl NCH₃ 3343 C₂H₅ n-C₄H₉ Cl NCH₃ 3344 C₂H₅ i-C₄H₉ Cl NCH₃ 3345 C₂H₅ s-C₄H₉ Cl NCH₃ 3346 C₂H₅ t-C₄H₉ Cl NCH₃ 3347 C₂H₅ CH₂OCH₃ Cl NCH₃ 3348 C₂H₅ CF₃ Cl NCH₃ 3349 C₂H₅ CF₂H Cl NCH₃ 3350 C₂H₅ CN Cl NCH₃ 3351 C₂H₅ OH Cl NCH₃ 3352 C₂H₅ OCH₃ Cl NCH₃ 3353 C₂H₅ NH₂ Cl NCH₃ 3354 C₂H₅ NHCH₃ Cl NCH₃ 3355 C₂H₅ N(CH₃)₂ Cl NCH₃ 3356 C₂H₅ CO₂CH₃ Cl NCH₃ 3357 C₂H₅ CO₂C₂H₅ Cl NCH₃ 3358 C₂H₅ C(O)CH₃ Cl NCH₃ 3359 C₂H₅ C(O)CF₃ Cl NCH₃ 3360 C₂H₅ C(═NOCH₃)CH₃ Cl NCH₃ 3361 C₂H₅ SO₂CH₃ Cl NCH₃ 3362 C₂H₅ SO₂CF₃ Cl NCH₃ 3363 C₂H₅ CH₂CO₂H Cl NCH₃ 3364 C₂H₅ CH₂COOCH₃ Cl NCH₃ 3365 C₂H₅ CH₂COOC₂H₅ Cl NCH₃ 3366 C₂H₅ prop-1-en-3-yl Cl NCH₃ 3367 C₂H₅ trans-but-2-en-1-yl Cl NCH₃ 3368 C₂H₅ cis-but-2-en-1-yl Cl NCH₃ 3369 C₂H₅ cis-3-methyl- Cl NCH₃ but-2-en-1-yl 3370 C₂H₅ cyclopropyl Cl NCH₃ 3371 C₂H₅ cyclopentyl Cl NCH₃ 3372 C₂H₅ cyclohexyl Cl NCH₃ 3373 C₂H₅ 4,5-dihydroisoxazol- Cl NCH₃ 3-yl 3374 C₂H₅ 4-methyl-4,5-dihydroisoxazol- Cl NCH₃ 3-yl 3375 C₂H₅ isoxazol-3-yl Cl NCH₃ 3376 C₂H₅ 4-methylisoxazol-3-yl Cl NCH₃ 3377 C₂H₅ 4,5-dihydroisoxazol- Cl NCH₃ 4-yl 3378 C₂H₅ 3-methyl-4,5-dihydroisoxazol- Cl NCH₃ 4-yl 3379 C₂H₅ isoxazol-4-yl Cl NCH₃ 3380 C₂H₅ 3-methylisoxazol-4-yl Cl NCH₃ 3381 C₂H₅ phenyl Cl NCH₃ 3382 C₂H₅ benzyl Cl NCH₃ 3383 C₂H₅ benzoyl Cl NCH₃ 3384 C₂H₅ 2-pyridyl Cl NCH₃ 3385 CH₃ n-pentyl H O 3386 CH₃ CH₂—C≡C—CH₂—CH₃ H O 3387 CH₃ CH₂—CH₂—CH═CH₂ H O 3388 CH₃ CH₂—CH₂—CH₂—CH═CH₂ H O 3389 CH₃ CH₂-[(3-OCH₃)C₆H₄] H O 3390 CH₃ CH₂—C≡C—CH₃ H O 3391 CH₃ CH₂—CH₂-(1,3-dioxolan- H O 2-yl) 3392 CH₃ CH₂-(1,3-dioxolan- H O 2-yl) 3393 CH₃ n-pentyl CH₃ O 3394 CH₃ CH₂—C≡C—CH₂—CH₃ CH₃ O 3395 CH₃ CH₂—CH₂—CH═CH₂ CH₃ O 3396 CH₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ O 3397 CH₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ O 3398 CH₃ CH₂—C≡C—CH₃ CH₃ O 3399 CH₃ CH₂—CH₂-(1,3-dioxolan- CH₃ O 2-yl) 3400 CH₃ CH₂-(1,3-dioxolan- CH₃ O 2-yl) 3401 CH₃ n-pentyl Cl O 3402 CH₃ CH₂—C≡C—CH₂—CH₃ Cl O 3403 CH₃ CH₂—CH₂—CH═CH₂ Cl O 3404 CH₃ CH₂—CH₂—CH₂—CH═CH₂ Cl O 3405 CH₃ CH₂-[(3-OCH₃)C₆H₄] Cl O 3406 CH₃ CH₂—C≡C—CH₃ Cl O 3407 CH₃ CH₂—CH₂-(1,3-dioxolan- Cl O 2-yl) 3408 CH₃ CH₂-(1,3-dioxolan- Cl O 2-yl) 3409 Cl n-pentyl H O 3410 Cl CH₂—C≡C—CH₂—CH₃ H O 3411 Cl CH₂—CH₂—CH═CH₂ H O 3412 Cl CH₂—CH₂—CH₂—CH═CH₂ H O 3413 Cl CH₂-[(3-OCH₃)C₆H₄] H O 3414 Cl CH₂—C≡C—CH₃ H O 3415 Cl CH₂—CH₂-(1,3-dioxolan- H O 2-yl) 3416 Cl CH₂-(1,3-dioxolan- H O 2-yl) 3417 Cl n-pentyl CH₃ O 3418 Cl CH₂—C≡C—CH₂—CH₃ CH₃ O 3419 Cl CH₂—CH₂—CH═CH₂ CH₃ O 3420 Cl CH₂—CH₂—CH₂—CH═CH₂ CH₃ O 3421 Cl CH₂-[(3-OCH₃)C₆H₄] CH₃ O 3422 Cl CH₂—C≡C—CH₃ CH₃ O 3423 Cl CH₂—CH₂-(1,3-dioxolan- CH₃ O 2-yl) 3424 Cl CH₂-(1,3-dioxolan- CH₃ O 2-yl) 3425 Cl n-pentyl Cl O 3426 Cl CH₂—C≡C—CH₂—CH₃ Cl O 3427 Cl CH₂—CH₂—CH═CH₂ Cl O 3428 Cl CH₂—CH₂—CH₂—CH═CH₂ Cl O 3429 Cl CH₂-[(3-OCH₃)C₆H₄] Cl O 3430 Cl CH₂—C≡C—CH₃ Cl O 3431 Cl CH₂—CH₂-(1,3-dioxolan- Cl O 2-yl) 3432 Cl CH₂-(1,3-dioxolan- Cl O 2-yl) 3433 OCH₃ n-pentyl H O 3434 OCH₃ CH₂—C≡C—CH₂—CH₃ H O 3435 OCH₃ CH₂—CH₂—CH═CH₂ H O 3436 OCH₃ CH₂—CH₂—CH₂—CH═CH₂ H O 3437 OCH₃ CH₂-[(3-OCH₃)C₆H₄] H O 3438 OCH₃ CH₂—C≡C—CH₃ H O 3439 OCH₃ CH₂—CH₂-(1,3-dioxolan- H O 2-yl) 3440 OCH₃ CH₂-(1,3-dioxolan- H O 2-yl) 3441 OCH₃ n-pentyl CH₃ O 3442 OCH₃ CH₂—C≡C—CH₂—CH₃ CH₃ O 3443 OCH₃ CH₂—CH₂—CH═CH₂ CH₃ O 3444 OCH₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ O 3445 OCH₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ O 3446 OCH₃ CH₂—C≡C—CH₃ CH₃ O 3447 OCH₃ CH₂—CH₂-(1,3-dioxolan- CH₃ O 2-yl) 3448 OCH₃ CH₂-(1,3-dioxolan- CH₃ O 2-yl) 3449 OCH₃ n-pentyl Cl O 3450 OCH₃ CH₂—C≡C—CH₂—CH₃ Cl O 3451 OCH₃ CH₂—CH₂—CH═CH₂ Cl O 3452 OCH₃ CH₂—CH₂—CH₂—CH═CH₂ Cl O 3453 OCH₃ CH₂-[(3-OCH₃)C₆H₄] Cl O 3454 OCH₃ CH₂—C≡C—CH₃ Cl O 3455 OCH₃ CH₂—CH₂-(1,3-dioxolan- Cl O 2-yl) 3456 OCH₃ CH₂-(1,3-dioxolan- Cl O 2-yl) 3457 OCF₃ n-pentyl H O 3458 OCF₃ CH₂—C≡C—CH₂—CH₃ H O 3459 OCF₃ CH₂—CH₂—CH═CH₂ H O 3460 OCF₃ CH₂—CH₂—CH₂—CH═CH₂ H O 3461 OCF₃ CH₂-[(3-OCH₃)C₆H₄] H O 3462 OCF₃ CH₂—C≡C—CH₃ H O 3463 OCF₃ CH₂—CH₂-(1,3-dioxolan- H O 2-yl) 3464 OCF₃ CH₂-(1,3-dioxolan- H O 2-yl) 3465 OCF₃ n-pentyl CH₃ O 3466 OCF₃ CH₂—C≡C—CH₂—CH₃ CH₃ O 3467 OCF₃ CH₂—CH₂—CH═CH₂ CH₃ O 3468 OCF₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ O 3469 OCF₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ O 3470 OCF₃ CH₂—C≡C—CH₃ CH₃ O 3471 OCF₃ CH₂—CH₂-(1,3-dioxolan- CH₃ O 2-yl) 3472 OCF₃ CH₂-(1,3-dioxolan- CH₃ O 2-yl) 3473 OCF₃ n-pentyl Cl O 3474 OCF₃ CH₂—C≡C—CH₂—CH₃ Cl O 3475 OCF₃ CH₂—CH₂—CH═CH₂ Cl O 3476 OCF₃ CH₂—CH₂—CH₂—CH═CH₂ Cl O 3477 OCF₃ CH₂-[(3-OCH₃)C₆H₄] Cl O 3478 OCF₃ CH₂—C≡C—CH₃ Cl O 3479 OCF₃ CH₂—CH₂-(1,3-dioxolan- Cl O 2-yl) 3480 OCF₃ CH₂-(1,3-dioxolan- Cl O 2-yl) 3481 SCH₃ n-pentyl H O 3482 SCH₃ CH₂—C≡C—CH₂—CH₃ H O 3483 SCH₃ CH₂—CH₂—CH═CH₂ H O 3484 SCH₃ CH₂—CH₂—CH₂—CH═CH₂ H O 3485 SCH₃ CH₂-[(3-OCH₃)C₆H₄] H O 3486 SCH₃ CH₂—C≡C—CH₃ H O 3487 SCH₃ CH₂—CH₂-(1,3-dioxolan- H O 2-yl) 3488 SCH₃ CH₂-(1,3-dioxolan- H O 2-yl) 3489 SCH₃ n-pentyl CH₃ O 3490 SCH₃ CH₂—C≡C—CH₂—CH₃ CH₃ O 3491 SCH₃ CH₂—CH₂—CH═CH₂ CH₃ O 3492 SCH₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ O 3493 SCH₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ O 3494 SCH₃ CH₂—C≡C—CH₃ CH₃ O 3495 SCH₃ CH₂—CH₂-(1,3-dioxolan- CH₃ O 2-yl) 3496 SCH₃ CH₂-(1,3-dioxolan- CH₃ O 2-yl) 3497 SCH₃ n-pentyl Cl O 3498 SCH₃ CH₂—C≡C—CH₂—CH₃ Cl O 3499 SCH₃ CH₂—CH₂—CH═CH₂ Cl O 3500 SCH₃ CH₂—CH₂—CH₂—CH═CH₂ Cl O 3501 SCH₃ CH₂-[(3-OCH₃)C₆H₄] Cl O 3502 SCH₃ CH₂—C≡C—CH₃ Cl O 3503 SCH₃ CH₂—CH₂-(1,3-dioxolan- Cl O 2-yl) 3504 SCH₃ CH₂-(1,3-dioxolan- Cl O 2-yl) 3505 SO₂CH₃ n-pentyl H O 3506 SO₂CH₃ CH₂—C≡C—CH₂—CH₃ H O 3507 SO₂CH₃ CH₂—CH₂—CH═CH₂ H O 3508 SO₂CH₃ CH₂—CH₂—CH₂—CH═CH₂ H O 3509 SO₂CH₃ CH₂-[(3-OCH₃)C₆H₄] H O 3510 SO₂CH₃ CH₂—C≡C—CH₃ H O 3511 SO₂CH₃ CH₂—CH₂-(1,3-dioxolan- H O 2-yl) 3512 SO₂CH₃ CH₂-(1,3-dioxolan- H O 2-yl) 3513 SO₂CH₃ n-pentyl CH₃ O 3514 SO₂CH₃ CH₂—C≡C—CH₂—CH₃ CH₃ O 3515 SO₂CH₃ CH₂—CH₂—CH═CH₂ CH₃ O 3516 SO₂CH₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ O 3517 SO₂CH₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ O 3518 SO₂CH₃ CH₂—C≡C—CH₃ CH₃ O 3519 SO₂CH₃ CH₂—CH₂-(1,3-dioxolan- CH₃ O 2-yl) 3520 SO₂CH₃ CH₂-(1,3-dioxolan- CH₃ O 2-yl) 3521 SO₂CH₃ n-pentyl Cl O 3522 SO₂CH₃ CH₂—C≡C—CH₂—CH₃ Cl O 3523 SO₂CH₃ CH₂—CH₂—CH═CH₂ Cl O 3524 SO₂CH₃ CH₂—CH₂—CH₂—CH═CH₂ Cl O 3525 SO₂CH₃ CH₂-[(3-OCH₃)C₆H₄] Cl O 3526 SO₂CH₃ CH₂—C≡C—CH₃ Cl O 3527 SO₂CH₃ CH₂—CH₂-(1,3-dioxolan- Cl O 2-yl) 3528 SO₂CH₃ CH₂-(1,3-dioxolan- Cl O 2-yl) 3529 CF₃ n-pentyl H O 3530 CF₃ CH₂—C≡C—CH₂—CH₃ H O 3531 CF₃ CH₂—CH₂—CH═CH₂ H O 3532 CF₃ CH₂—CH₂—CH₂—CH═CH₂ H O 3533 CF₃ CH₂-[(3-OCH₃)C₆H₄] H O 3534 CF₃ CH₂—C≡C—CH₃ H O 3535 CF₃ CH₂—CH₂-(1,3-dioxolan- H O 2-yl) 3536 CF₃ CH₂-(1,3-dioxolan- H O 2-yl) 3537 CF₃ n-pentyl CH₃ O 3538 CF₃ CH₂—C≡C—CH₂—CH₃ CH₃ O 3539 CF₃ CH₂—CH₂—CH═CH₂ CH₃ O 3540 CF₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ O 3541 CF₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ O 3542 CF₃ CH₂—C≡C—CH₃ CH₃ O 3543 CF₃ CH₂—CH₂-(1,3-dioxolan- CH₃ O 2-yl) 3544 CF₃ CH₂-(1,3-dioxolan- CH₃ O 2-yl) 3545 CF₃ n-pentyl Cl O 3546 CF₃ CH₂—C≡C—CH₂—CH₃ Cl O 3547 CF₃ CH₂—CH₂—CH═CH₂ Cl O 3548 CF₃ CH₂—CH₂—CH₂—CH═CH₂ Cl O 3549 CF₃ CH₂-[(3-OCH₃)C₆H₄] Cl O 3550 CF₃ CH₂—C≡C—CH₃ Cl O 3551 CF₃ CH₂—CH₂-(1,3-dioxolan- Cl O 2-yl) 3552 CF₃ CH₂-(1,3-dioxolan- Cl O 2-yl) 3553 C₂H₅ n-pentyl H O 3554 C₂H₅ CH₂—C≡C—CH₂—CH₃ H O 3555 C₂H₅ CH₂—CH₂—CH═CH₂ H O 3556 C₂H₅ CH₂—CH₂—CH₂—CH═CH₂ H O 3557 C₂H₅ CH₂-[(3-OCH₃)C₆H₄] H O 3558 C₂H₅ CH₂—C≡C—CH₃ H O 3559 C₂H₅ CH₂—CH₂-(1,3-dioxolan- H O 2-yl) 3560 C₂H₅ CH₂-(1,3-dioxolan- H O 2-yl) 3561 C₂H₅ n-pentyl CH₃ O 3562 C₂H₅ CH₂—C≡C—CH₂—CH₃ CH₃ O 3563 C₂H₅ CH₂—CH₂—CH═CH₂ CH₃ O 3564 C₂H₅ CH₂—CH₂—CH₂—CH═CH₂ CH₃ O 3565 C₂H₅ CH₂-[(3-OCH₃)C₆H₄] CH₃ O 3566 C₂H₅ CH₂—C≡C—CH₃ CH₃ O 3567 C₂H₅ CH₂—CH₂-(1,3-dioxolan- CH₃ O 2-yl) 3568 C₂H₅ CH₂-(1,3-dioxolan- CH₃ O 2-yl) 3569 C₂H₅ n-pentyl Cl O 3570 C₂H₅ CH₂—C≡C—CH₂—CH₃ Cl O 3571 C₂H₅ CH₂—CH₂—CH═CH₂ Cl O 3572 C₂H₅ CH₂—CH₂—CH₂—CH═CH₂ Cl O 3573 C₂H₅ CH₂-[(3-OCH₃)C₆H₄] Cl O 3574 C₂H₅ CH₂—C≡C—CH₃ Cl O 3575 C₂H₅ CH₂—CH₂-(1,3-dioxolan- Cl O 2-yl) 3576 C₂H₅ CH₂-(1,3-dioxolan- Cl O 2-yl) 3577 CH₃ n-pentyl H S 3578 CH₃ CH₂—C≡C—CH₂—CH₃ H S 3579 CH₃ CH₂—CH₂—CH═CH₂ H S 3580 CH₃ CH₂—CH₂—CH₂—CH═CH₂ H S 3581 CH₃ CH₂-[(3-OCH₃)C₆H₄] H S 3582 CH₃ CH₂—C≡C—CH₃ H S 3583 CH₃ CH₂—CH₂-(1,3-dioxolan- H S 2-yl) 3584 CH₃ CH₂-(1,3-dioxolan- H S 2-yl) 3585 CH₃ n-pentyl CH₃ S 3586 CH₃ CH₂—C≡C—CH₂—CH₃ CH₃ S 3587 CH₃ CH₂—CH₂—CH═CH₂ CH₃ S 3588 CH₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ S 3589 CH₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ S 3590 CH₃ CH₂—C≡C—CH₃ CH₃ S 3591 CH₃ CH₂—CH₂-(1,3-dioxolan- CH₃ S 2-yl) 3592 CH₃ CH₂-(1,3-dioxolan- CH₃ S 2-yl) 3593 CH₃ n-pentyl Cl S 3594 CH₃ CH₂—C≡C—CH₂—CH₃ Cl S 3595 CH₃ CH₂—CH₂—CH═CH₂ Cl S 3596 CH₃ CH₂—CH₂—CH₂—CH═CH₂ Cl S 3597 CH₃ CH₂-[(3-OCH₃)C₆H₄] Cl S 3598 CH₃ CH₂—C≡C—CH₃ Cl S 3599 CH₃ CH₂—CH₂-(1,3-dioxolan- Cl S 2-yl) 3600 CH₃ CH₂-(1,3-dioxolan- Cl S 2-yl) 3601 Cl n-pentyl H S 3602 Cl CH₂—C≡C—CH₂—CH₃ H S 3603 Cl CH₂—CH₂—CH═CH₂ H S 3604 Cl CH₂—CH₂—CH₂—CH═CH₂ H S 3605 Cl CH₂-[(3-OCH₃)C₆H₄] H S 3606 Cl CH₂—C≡C—CH₃ H S 3607 Cl CH₂—CH₂-(1,3-dioxolan- H S 2-yl) 3608 Cl CH₂-(1,3-dioxolan- H S 2-yl) 3609 Cl n-pentyl CH₃ S 3610 Cl CH₂—C≡C—CH₂—CH₃ CH₃ S 3611 Cl CH₂—CH₂—CH═CH₂ CH₃ S 3612 Cl CH₂—CH₂—CH₂—CH═CH₂ CH₃ S 3613 Cl CH₂-[(3-OCH₃)C₆H₄] CH₃ S 3614 Cl CH₂—C≡C—CH₃ CH₃ S 3615 Cl CH₂—CH₂-(1,3-dioxolan- CH₃ S 2-yl) 3616 Cl CH₂-(1,3-dioxolan- CH₃ S 2-yl) 3617 Cl n-pentyl Cl S 3618 Cl CH₂—C≡C—CH₂—CH₃ Cl S 3619 Cl CH₂—CH₂—CH═CH₂ Cl S 3620 Cl CH₂—CH₂—CH₂—CH═CH₂ Cl S 3621 Cl CH₂-[(3-OCH₃)C₆H₄] Cl S 3622 Cl CH₂—C≡C—CH₃ Cl S 3623 Cl CH₂—CH₂-(1,3-dioxolan- Cl S 2-yl) 3624 Cl CH₂-(1,3-dioxolan- Cl S 2-yl) 3625 OCH₃ n-pentyl H S 3626 OCH₃ CH₂—C≡C—CH₂—CH₃ H S 3627 OCH₃ CH₂—CH₂—CH═CH₂ H S 3628 OCH₃ CH₂—CH₂—CH₂—CH═CH₂ H S 3629 OCH₃ CH₂-[(3-OCH₃)C₆H₄] H S 3630 OCH₃ CH₂—C≡C—CH₃ H S 3631 OCH₃ CH₂—CH₂-(1,3-dioxolan- H S 2-yl) 3632 OCH₃ CH₂-(1,3-dioxolan- H S 2-yl) 3633 OCH₃ n-pentyl CH₃ S 3634 OCH₃ CH₂—C≡C—CH₂—CH₃ CH₃ S 3635 OCH₃ CH₂—CH₂—CH═CH₂ CH₃ S 3636 OCH₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ S 3637 OCH₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ S 3638 OCH₃ CH₂—C≡C—CH₃ CH₃ S 3639 OCH₃ CH₂—CH₂-(1,3-dioxolan- CH₃ S 2-yl) 3640 OCH₃ CH₂-(1,3-dioxolan- CH₃ S 2-yl) 3641 OCH₃ n-pentyl Cl S 3642 OCH₃ CH₂—C≡C—CH₂—CH₃ Cl S 3643 OCH₃ CH₂—CH₂—CH═CH₂ Cl S 3644 OCH₃ CH₂—CH₂—CH₂—CH═CH₂ Cl S 3645 OCH₃ CH₂-[(3-OCH₃)C₆H₄] Cl S 3646 OCH₃ CH₂—C≡C—CH₃ Cl S 3647 OCH₃ CH₂—CH₂-(1,3-dioxolan- Cl S 2-yl) 3648 OCH₃ CH₂-(1,3-dioxolan- Cl S 2-yl) 3649 OCF₃ n-pentyl H S 3650 OCF₃ CH₂—C≡C—CH₂—CH₃ H S 3651 OCF₃ CH₂—CH₂—CH═CH₂ H S 3652 OCF₃ CH₂—CH₂—CH₂—CH═CH₂ H S 3653 OCF₃ CH₂-[(3-OCH₃)C₆H₄] H S 3654 OCF₃ CH₂—C≡C—CH₃ H S 3655 OCF₃ CH₂—CH₂-(1,3-dioxolan- H S 2-yl) 3656 OCF₃ CH₂-(1,3-dioxolan- H S 2-yl) 3657 OCF₃ n-pentyl CH₃ S 3658 OCF₃ CH₂—C≡C—CH₂—CH₃ CH₃ S 3659 OCF₃ CH₂—CH₂—CH═CH₂ CH₃ S 3660 OCF₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ S 3661 OCF₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ S 3662 OCF₃ CH₂—C≡C—CH₃ CH₃ S 3663 OCF₃ CH₂—CH₂-(1,3-dioxolan- CH₃ S 2-yl) 3664 OCF₃ CH₂-(1,3-dioxolan- CH₃ S 2-yl) 3665 OCF₃ n-pentyl Cl S 3666 OCF₃ CH₂—C≡C—CH₂—CH₃ Cl S 3667 OCF₃ CH₂—CH₂—CH═CH₂ Cl S 3668 OCF₃ CH₂—CH₂—CH₂—CH═CH₂ Cl S 3669 OCF₃ CH₂-[(3-OCH₃)C₆H₄] Cl S 3670 OCF₃ CH₂—C≡C—CH₃ Cl S 3671 OCF₃ CH₂—CH₂-(1,3-dioxolan- Cl S 2-yl) 3672 OCF₃ CH₂-(1,3-dioxolan- Cl S 2-yl) 3673 SCH₃ n-pentyl H S 3674 SCH₃ CH₂—C≡C—CH₂—CH₃ H S 3675 SCH₃ CH₂—CH₂—CH═CH₂ H S 3676 SCH₃ CH₂—CH₂—CH₂—CH═CH₂ H S 3677 SCH₃ CH₂-[(3-OCH₃)C₆H₄] H S 3678 SCH₃ CH₂—C≡C—CH₃ H S 3679 SCH₃ CH₂—CH₂-(1,3-dioxolan- H S 2-yl) 3680 SCH₃ CH₂-(1,3-dioxolan- H S 2-yl) 3681 SCH₃ n-pentyl CH₃ S 3682 SCH₃ CH₂—C≡C—CH₂—CH₃ CH₃ S 3683 SCH₃ CH₂—CH₂—CH═CH₂ CH₃ S 3684 SCH₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ S 3685 SCH₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ S 3686 SCH₃ CH₂—C≡C—CH₃ CH₃ S 3687 SCH₃ CH₂—CH₂-(1,3-dioxolan- CH₃ S 2-yl) 3688 SCH₃ CH₂-(1,3-dioxolan- CH₃ S 2-yl) 3689 SCH₃ n-pentyl Cl S 3690 SCH₃ CH₂—C≡C—CH₂—CH₃ Cl S 3691 SCH₃ CH₂—CH₂—CH═CH₂ Cl S 3692 SCH₃ CH₂—CH₂—CH₂—CH═CH₂ Cl S 3693 SCH₃ CH₂-[(3-OCH₃)C₆H₄] Cl S 3694 SCH₃ CH₂—C≡C—CH₃ Cl S 3695 SCH₃ CH₂—CH₂-(1,3-dioxolan- Cl S 2-yl) 3696 SCH₃ CH₂-(1,3-dioxolan- Cl S 2-yl) 3697 SO₂CH₃ n-pentyl H S 3698 SO₂CH₃ CH₂—C≡C—CH₂—CH₃ H S 3699 SO₂CH₃ CH₂—CH₂—CH═CH₂ H S 3700 SO₂CH₃ CH₂—CH₂—CH₂—CH═CH₂ H S 3701 SO₂CH₃ CH₂-[(3-OCH₃)C₆H₄] H S 3702 SO₂CH₃ CH₂—C≡C—CH₃ H S 3703 SO₂CH₃ CH₂—CH₂-(1,3-dioxolan- H S 2-yl) 3704 SO₂CH₃ CH₂-(1,3-dioxolan- H S 2-yl) 3705 SO₂CH₃ n-pentyl CH₃ S 3706 SO₂CH₃ CH₂—C≡C—CH₂—CH₃ CH₃ S 3707 SO₂CH₃ CH₂—CH₂—CH═CH₂ CH₃ S 3708 SO₂CH₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ S 3709 SO₂CH₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ S 3710 SO₂CH₃ CH₂—C≡C—CH₃ CH₃ S 3711 SO₂CH₃ CH₂—CH₂-(1,3-dioxolan- CH₃ S 2-yl) 3712 SO₂CH₃ CH₂-(1,3-dioxolan- CH₃ S 2-yl) 3713 SO₂CH₃ n-pentyl Cl S 3714 SO₂CH₃ CH₂—C≡C—CH₂—CH₃ Cl S 3715 SO₂CH₃ CH₂—CH₂—CH═CH₂ Cl S 3716 SO₂CH₃ CH₂—CH₂—CH₂—CH═CH₂ Cl S 3717 SO₂CH₃ CH₂-[(3-OCH₃)C₆H₄] Cl S 3718 SO₂CH₃ CH₂—C≡C—CH₃ Cl S 3719 SO₂CH₃ CH₂—CH₂-(1,3-dioxolan- Cl S 2-yl) 3720 SO₂CH₃ CH₂-(1,3-dioxolan- Cl S 2-yl) 3721 CF₃ n-pentyl H S 3722 CF₃ CH₂—C≡C—CH₂—CH₃ H S 3723 CF₃ CH₂—CH₂—CH═CH₂ H S 3724 CF₃ CH₂—CH₂—CH₂—CH═CH₂ H S 3725 CF₃ CH₂-[(3-OCH₃)C₆H₄] H S 3726 CF₃ CH₂—C≡C—CH₃ H S 3727 CF₃ CH₂—CH₂-(1,3-dioxolan- H S 2-yl) 3728 CF₃ CH₂-(1,3-dioxolan- H S 2-yl) 3729 CF₃ n-pentyl CH₃ S 3730 CF₃ CH₂—C≡C—CH₂—CH₃ CH₃ S 3731 CF₃ CH₂—CH₂—CH═CH₂ CH₃ S 3732 CF₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ S 3733 CF₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ S 3734 CF₃ CH₂—C≡C—CH₃ CH₃ S 3735 CF₃ CH₂—CH₂-(1,3-dioxolan- CH₃ S 2-yl) 3736 CF₃ CH₂-(1,3-dioxolan- CH₃ S 2-yl) 3737 CF₃ n-pentyl Cl S 3738 CF₃ CH₂—C≡C—CH₂—CH₃ Cl S 3739 CF₃ CH₂—CH₂—CH═CH₂ Cl S 3740 CF₃ CH₂—CH₂—CH₂—CH═CH₂ Cl S 3741 CF₃ CH₂-[(3-OCH₃)C₆H₄] Cl S 3742 CF₃ CH₂—C≡C—CH₃ Cl S 3743 CF₃ CH₂—CH₂-(1,3-dioxolan Cl S 2-yl) 3744 CF₃ CH₂-(1,3-dioxolan- Cl S 2-yl) 3745 C₂H₅ n-pentyl H S 3746 C₂H₅ CH₂—C≡C—CH₂—CH₃ H S 3747 C₂H₅ CH₂—CH₂—CH═CH₂ H S 3748 C₂H₅ CH₂—CH₂—CH₂—CH═CH₂ H S 3749 C₂H₅ CH₂-[(3-OCH₃)C₆H₄] H S 3750 C₂H₅ CH₂—C≡C—CH₃ H S 3751 C₂H₅ CH₂—CH₂-(1,3-dioxolan- H S 2-yl) 3752 C₂H₅ CH₂-(1,3-dioxolan- H S 2-yl) 3753 C₂H₅ n-pentyl CH₃ S 3754 C₂H₅ CH₂—C≡C—CH₂—CH₃ CH₃ S 3755 C₂H₅ CH₂—CH₂—CH═CH₂ CH₃ S 3756 C₂H₅ CH₂—CH₂—CH₂—CH═CH₂ CH₃ S 3757 C₂H₅ CH₂-[(3-OCH₃)C₆H₄] CH₃ S 3758 C₂H₅ CH₂—C≡C—CH₃ CH₃ S 3759 C₂H₅ CH₂—CH₂-(1,3-dioxolan- CH₃ S 2-yl) 3760 C₂H₅ CH₂-(1,3-dioxolan- CH₃ S 2-yl) 3761 C₂H₅ n-pentyl Cl S 3762 C₂H₅ CH₂—C≡C—CH₂—CH₃ Cl S 3763 C₂H₅ CH₂—CH₂—CH═CH₂ Cl S 3764 C₂H₅ CH₂—CH₂—CH₂—CH═CH₂ Cl S 3765 C₂H₅ CH₂-[(3-OCH₃)C₆H₄] Cl S 3766 C₂H₅ CH₂—C≡C—CH₃ Cl S 3767 C₂H₅ CH₂—CH₂-(1,3-dioxolan- Cl S 2-yl) 3768 C₂H₅ CH₂-(1,3-dioxolan- Cl S 2-yl) 3769 CH₃ n-pentyl H NCH₃ 3770 CH₃ CH₂—C≡C—CH₂—CH₃ H NCH₃ 3771 CH₃ CH₂—CH₂—CH═CH₂ H NCH₃ 3772 CH₃ CH₂—CH₂—CH₂—CH═CH₂ H NCH₃ 3773 CH₃ CH₂-[(3-OCH₃)C₆H₄] H NCH₃ 3774 CH₃ CH₂—C≡C—CH₃ H NCH₃ 3775 CH₃ CH₂—CH₂-(1,3-dioxolan- H NCH₃ 2-yl) 3776 CH₃ CH₂-(1,3-dioxolan- H NCH₃ 2-yl) 3777 CH₃ n-pentyl CH₃ NCH₃ 3778 CH₃ CH₂—C≡C—CH₂—CH₃ CH₃ NCH₃ 3779 CH₃ CH₂—CH₂—CH═CH₂ CH₃ NCH₃ 3780 CH₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ NCH₃ 3781 CH₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ NCH₃ 3782 CH₃ CH₂—C≡C—CH₃ CH₃ NCH₃ 3783 CH₃ CH₂—CH₂-(1,3-dioxolan- CH₃ NCH₃ 2-yl) 3784 CH₃ CH₂-(1,3-dioxolan- CH₃ NCH₃ 2-yl) 3785 CH₃ n-pentyl Cl NCH₃ 3786 CH₃ CH₂—C≡C—CH₂—CH₃ Cl NCH₃ 3787 CH₃ CH₂—CH₂—CH═CH₂ Cl NCH₃ 3788 CH₃ CH₂—CH₂—CH₂—CH═CH₂ Cl NCH₃ 3789 CH₃ CH₂-[(3-OCH₃)C₆H₄] Cl NCH₃ 3790 CH₃ CH₂—C≡C—CH₃ Cl NCH₃ 3791 CH₃ CH₂—CH₂-(1,3-dioxolan- Cl NCH₃ 2-yl) 3792 CH₃ CH₂-(1,3-dioxolan- Cl NCH₃ 2-yl) 3793 Cl n-pentyl H NCH₃ 3794 Cl CH₂—C≡C—CH₂—CH₃ H NCH₃ 3795 Cl CH₂—CH₂—CH═CH₂ H NCH₃ 3796 Cl CH₂—CH₂—CH₂—CH═CH₂ H NCH₃ 3797 Cl CH₂-[(3-OCH₃)C₆H₄] H NCH₃ 3798 Cl CH₂—C≡C—CH₃ H NCH₃ 3799 Cl CH₂—CH₂-(1,3-dioxolan- H NCH₃ 2-yl) 3800 Cl CH₂-(1,3-dioxolan- H NCH₃ 2-yl) 3801 Cl n-pentyl CH₃ NCH₃ 3802 Cl CH₂—C≡C—CH₂—CH₃ CH₃ NCH₃ 3803 Cl CH₂—CH₂—CH═CH₂ CH₃ NCH₃ 3804 Cl CH₂—CH₂—CH₂—CH═CH₂ CH₃ NCH₃ 3805 Cl CH₂-[(3-OCH₃)C₆H₄] CH₃ NCH₃ 3806 Cl CH₂—C≡C—CH₃ CH₃ NCH₃ 3807 Cl CH₂—CH₂-(1,3-dioxolan- CH₃ NCH₃ 2-yl) 3808 Cl CH₂-(1,3-dioxolan- CH₃ NCH₃ 2-yl) 3809 Cl n-pentyl Cl NCH₃ 3810 Cl CH₂—C≡C—CH₂—CH₃ Cl NCH₃ 3811 Cl CH₂—CH₂—CH═CH₂ Cl NCH₃ 3812 Cl CH₂—CH₂—CH₂—CH═CH₂ Cl NCH₃ 3813 Cl CH₂-[(3-OCH₃)C₆H₄] Cl NCH₃ 3814 Cl CH₂—C≡C—CH₃ Cl NCH₃ 3815 Cl CH₂—CH₂-(1,3-dioxolan- Cl NCH₃ 2-yl) 3816 Cl CH₂-(1,3-dioxolan- Cl NCH₃ 2-yl) 3817 OCH₃ n-pentyl H NCH₃ 3818 OCH₃ CH₂—C≡C—CH₂—CH₃ H NCH₃ 3819 OCH₃ CH₂—CH₂—CH═CH₂ H NCH₃ 3820 OCH₃ CH₂—CH₂—CH₂—CH═CH₂ H NCH₃ 3821 OCH₃ CH₂-[(3-OCH₃)C₆H₄] H NCH₃ 3822 OCH₃ CH₂—C≡C—CH₃ H NCH₃ 3823 OCH₃ CH₂—CH₂-(1,3-dioxolan- H NCH₃ 2-yl) 3824 OCH₃ CH₂-(1,3-dioxolan- H NCH₃ 2-yl) 3825 OCH₃ n-pentyl CH₃ NCH₃ 3826 OCH₃ CH₂—C≡C—CH₂—CH₃ CH₃ NCH₃ 3827 OCH₃ CH₂—CH₂—CH═CH₂ CH₃ NCH₃ 3828 OCH₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ NCH₃ 3829 OCH₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ NCH₃ 3830 OCH₃ CH₂—C≡C—CH₃ CH₃ NCH₃ 3831 OCH₃ CH₂—CH₂-(1,3-dioxolan- CH₃ NCH₃ 2-yl) 3832 OCH₃ CH₂-(1,3-dioxolan- CH₃ NCH₃ 2-yl) 3833 OCH₃ n-pentyl Cl NCH₃ 3834 OCH₃ CH₂—C≡C—CH₂—CH₃ Cl NCH₃ 3835 OCH₃ CH₂—CH₂—CH═CH₂ Cl NCH₃ 3836 OCH₃ CH₂—CH₂—CH₂—CH═CH₂ Cl NCH₃ 3837 OCH₃ CH₂-[(3-OCH₃)C₆H₄] Cl NCH₃ 3838 OCH₃ CH₂—C≡C—CH₃ Cl NCH₃ 3839 OCH₃ CH₂—CH₂-(1,3-dioxolan- Cl NCH₃ 2-yl) 3840 OCH₃ CH₂-(1,3-dioxolan- Cl NCH₃ 2-yl) 3841 OCF₃ n-pentyl H NCH₃ 3842 OCF₃ CH₂—C≡C—CH₂—CH₃ H NCH₃ 3843 OCF₃ CH₂—CH₂—CH═CH₂ H NCH₃ 3844 OCF₃ CH₂—CH₂—CH₂—CH═CH₂ H NCH₃ 3845 OCF₃ CH₂-[(3-OCH₃)C₆H₄] H NCH₃ 3846 OCF₃ CH₂—C≡C—CH₃ H NCH₃ 3847 OCF₃ CH₂—CH₂-(1,3-dioxolan- H NCH₃ 2-yl) 3848 OCF₃ CH₂-(1,3-dioxolan- H NCH₃ 2-yl) 3849 OCF₃ n-pentyl CH₃ NCH₃ 3850 OCF₃ CH₂—C≡C—CH₂—CH₃ CH₃ NCH₃ 3851 OCF₃ CH₂—CH₂—CH═CH₂ CH₃ NCH₃ 3852 OCF₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ NCH₃ 3853 OCF₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ NCH₃ 3854 OCF₃ CH₂—C≡C—CH₃ CH₃ NCH₃ 3855 OCF₃ CH₂—CH₂-(1,3-dioxolan- CH₃ NCH₃ 2-yl) 3856 OCF₃ CH₂-(1,3-dioxolan- CH₃ NCH₃ 2-yl) 3857 OCF₃ n-pentyl Cl NCH₃ 3858 OCF₃ CH₂—C≡C—CH₂—CH₃ Cl NCH₃ 3859 OCF₃ CH₂—CH₂—CH═CH₂ Cl NCH₃ 3860 OCF₃ CH₂—CH₂—CH₂—CH═CH₂ Cl NCH₃ 3861 OCF₃ CH₂-[(3-OCH₃)C₆H₄] Cl NCH₃ 3862 OCF₃ CH₂—C≡C—CH₃ Cl NCH₃ 3863 OCF₃ CH₂—CH₂-(1,3-dioxolan- Cl NCH₃ 2-yl) 3864 OCF₃ CH₂-(1,3-dioxolan- Cl NCH₃ 2-yl) 3865 SCH₃ n-pentyl H NCH₃ 3866 SCH₃ CH₂—C≡C—CH₂—CH₃ H NCH₃ 3867 SCH₃ CH₂—CH₂—CH═CH₂ H NCH₃ 3868 SCH₃ CH₂—CH₂—CH₂—CH═CH₂ H NCH₃ 3869 SCH₃ CH₂-[(3-OCH₃)C₆H₄] H NCH₃ 3870 SCH₃ CH₂—C≡C—CH₃ H NCH₃ 3871 SCH₃ CH₂—CH₂-(1,3-dioxolan- H NCH₃ 2-yl) 3872 SCH₃ CH₂-(1,3-dioxolan- H NCH₃ 2-yl) 3873 SCH₃ n-pentyl CH₃ NCH₃ 3874 SCH₃ CH₂—C≡C—CH₂—CH₃ CH₃ NCH₃ 3875 SCH₃ CH₂—CH₂—CH═CH₂ CH₃ NCH₃ 3876 SCH₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ NCH₃ 3877 SCH₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ NCH₃ 3878 SCH₃ CH₂—C≡C—CH₃ CH₃ NCH₃ 3879 SCH₃ CH₂—CH₂-(1,3-dioxolan- CH₃ NCH₃ 2-yl) 3880 SCH₃ CH₂-(1,3-dioxolan- CH₃ NCH₃ 2-yl) 3881 SCH₃ n-pentyl Cl NCH₃ 3882 SCH₃ CH₂—C≡C—CH₂—CH₃ Cl NCH₃ 3883 SCH₃ CH₂—CH₂—CH═CH₂ Cl NCH₃ 3884 SCH₃ CH₂—CH₂—CH₂—CH═CH₂ Cl NCH₃ 3885 SCH₃ CH₂-[(3-OCH₃)C₆H₄] Cl NCH₃ 3886 SCH₃ CH₂—C≡C—CH₃ Cl NCH₃ 3887 SCH₃ CH₂—CH₂-(1,3-dioxolan- Cl NCH₃ 2-yl) 3888 SCH₃ CH₂-(1,3-dioxolan- Cl NCH₃ 2-yl) 3889 SO₂CH₃ n-pentyl H NCH₃ 3890 SO₂CH₃ CH₂—C≡C—CH₂—CH₃ H NCH₃ 3891 SO₂CH₃ CH₂—CH₂—CH═CH₂ H NCH₃ 3892 SO₂CH₃ CH₂—CH₂—CH₂—CH═CH₂ H NCH₃ 3893 SO₂CH₃ CH₂-[(3-OCH₃)C₆H₄] H NCH₃ 3894 SO₂CH₃ CH₂—C≡C—CH₃ H NCH₃ 3895 SO₂CH₃ CH₂—CH₂-(1,3-dioxolan- H NCH₃ 2-yl) 3896 SO₂CH₃ CH₂-(1,3-dioxolan- H NCH₃ 2-yl) 3897 SO₂CH₃ n-pentyl CH₃ NCH₃ 3898 SO₂CH₃ CH₂—C≡C—CH₂—CH₃ CH₃ NCH₃ 3899 SO₂CH₃ CH₂—CH₂—CH═CH₂ CH₃ NCH₃ 3900 SO₂CH₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ NCH₃ 3901 SO₂CH₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ NCH₃ 3902 SO₂CH₃ CH₂—C≡C—CH₃ CH₃ NCH₃ 3903 SO₂CH₃ CH₂—CH₂-(1,3-dioxolan- CH₃ NCH₃ 2-yl) 3904 SO₂CH₃ CH₂-(1,3-dioxolan- CH₃ NCH₃ 2-yl) 3905 SO₂CH₃ n-pentyl Cl NCH₃ 3906 SO₂CH₃ CH₂—C≡C—CH₂—CH₃ Cl NCH₃ 3907 SO₂CH₃ CH₂—CH₂—CH═CH₂ Cl NCH₃ 3908 SO₂CH₃ CH₂—CH₂—CH₂—CH═CH₂ Cl NCH₃ 3909 SO₂CH₃ CH₂-[(3-OCH₃)C₆H₄] Cl NCH₃ 3910 SO₂CH₃ CH₂—C≡C—CH₃ Cl NCH₃ 3911 SO₂CH₃ CH₂—CH₂-(1,3-dioxolan- Cl NCH₃ 2-yl) 3912 SO₂CH₃ CH₂-(1,3-dioxolan- Cl NCH₃ 2-yl) 3913 CF₃ n-pentyl H NCH₃ 3914 CF₃ CH₂—C≡C—CH₂—CH₃ H NCH₃ 3915 CF₃ CH₂—CH₂—CH═CH₂ H NCH₃ 3916 CF₃ CH₂—CH₂—CH₂—CH═CH₂ H NCH₃ 3917 CF₃ CH₂-[(3-OCH₃)C₆H₄] H NCH₃ 3918 CF₃ CH₂—C≡C—CH₃ H NCH₃ 3919 CF₃ CH₂—CH₂-(1,3-dioxolan- H NCH₃ 2-yl) 3920 CF₃ CH₂-(1,3-dioxolan- H NCH₃ 2-yl) 3921 CF₃ n-pentyl CH₃ NCH₃ 3922 CF₃ CH₂—C≡C—CH₂—CH₃ CH₃ NCH₃ 3923 CF₃ CH₂—CH₂—CH═CH₂ CH₃ NCH₃ 3924 CF₃ CH₂—CH₂—CH₂—CH═CH₂ CH₃ NCH₃ 3925 CF₃ CH₂-[(3-OCH₃)C₆H₄] CH₃ NCH₃ 3926 CF₃ CH₂—C≡C—CH₃ CH₃ NCH₃ 3927 CF₃ CH₂—CH₂-(1,3-dioxolan- CH₃ NCH₃ 2-yl) 3928 CF₃ CH₂-(1,3-dioxolan- CH₃ NCH₃ 2-yl) 3929 CF₃ n-pentyl Cl NCH₃ 3930 CF₃ CH₂—C≡C—CH₂—CH₃ Cl NCH₃ 3931 CF₃ CH₂—CH₂—CH═CH₂ Cl NCH₃ 3932 CF₃ CH₂—CH₂—CH₂—CH═CH₂ Cl NCH₃ 3933 CF₃ CH₂-[(3-OCH₃)C₆H₄] Cl NCH₃ 3934 CF₃ CH₂—C≡C—CH₃ Cl NCH₃ 3935 CF₃ CH₂—CH₂-(1,3-dioxolan- Cl NCH₃ 2-yl) 3936 CF₃ CH₂-(1,3-dioxolan- Cl NCH₃ 2-yl) 3937 C₂H₅ n-pentyl H NCH₃ 3938 C₂H₅ CH₂—C≡C—CH₂—CH₃ H NCH₃ 3939 C₂H₅ CH₂—CH₂—CH═CH₂ H NCH₃ 3940 C₂H₅ CH₂—CH₂—CH₂—CH═CH₂ H NCH₃ 3941 C₂H₅ CH₂-[(3-OCH₃)C₆H₄] H NCH₃ 3942 C₂H₅ CH₂—C≡C—CH₃ H NCH₃ 3943 C₂H₅ CH₂—CH₂-(1,3-dioxolan- H NCH₃ 2-yl) 3944 C₂H₅ CH₂-(1,3-dioxolan- H NCH₃ 2-yl) 3945 C₂H₅ n-pentyl CH₃ NCH₃ 3946 C₂H₅ CH₂—C≡C—CH₂—CH₃ CH₃ NCH₃ 3947 C₂H₅ CH₂—CH₂—CH═CH₂ CH₃ NCH₃ 3948 C₂H₅ CH₂—CH₂—CH₂—CH═CH₂ CH₃ NCH₃ 3949 C₂H₅ CH₂-[(3-OCH₃)C₆H₄] CH₃ NCH₃ 3950 C₂H₅ CH₂—C≡C—CH₃ CH₃ NCH₃ 3951 C₂H₅ CH₂—CH₂-(1,3-dioxolan- CH₃ NCH₃ 2-yl) 3952 C₂H₅ CH₂-(1,3-dioxolan- CH₃ NCH₃ 2-yl) 3953 C₂H₅ n-pentyl Cl NCH₃ 3954 C₂H₅ CH₂—C≡C—CH₂—CH₃ Cl NCH₃ 3955 C₂H₅ CH₂—CH₂—CH═CH₂ Cl NCH₃ 3956 C₂H₅ CH₂—CH₂—CH₂—CH═CH₂ Cl NCH₃ 3957 C₂H₅ CH₂-[(3-OCH₃)C₆H₄] Cl NCH₃ 3958 C₂H₅ CH₂—C≡C—CH₃ Cl NCH₃ 3959 C₂H₅ CH₂—CH₂-(1,3-dioxolan- Cl NCH₃ 2-yl) 3960 C₂H₅ CH₂-(1,3-dioxolan- Cl NCH₃ 2-yl)

Examples of particularly preferred benzothiazol-5-ylcarbonyl derivatives of cyclohexenones according to the invention are the compounds listed in Tables 1 to 28.

TABLE 1 Compounds I-1a.1 to I-1a.3960

I-1a

Compounds of the formula I-1a in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 2 Compounds I-1b.1 to I-1b.3960

I-1b

Compounds of the formula I-1b in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 3 Compounds I-1c.1 to I-1c.3960

I-1c

Compounds of the formula I-1c in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 4 Compounds I-1d.1 to I-1d.3960

I-1d

Compounds of the formula I-1d in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 5 Compounds I-1e.1 to I-1e.3960

I-1e

Compounds of the formula I-1e in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 6 Compounds I-1f.1 to I-1f.3960

I-1f

Compounds of the formula I-1f in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 7 Compounds I-1g.1 to I-1g.3960

I-1g

Compounds of the formula I-1g in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 8 Compounds I-1h.1 to I-1h.3960

I-1h

Compounds of the formula I-1h in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 9 Compounds I-1i.1 to I-1i.3960

I-1i

Compounds of the formula I-1i in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 10 Compounds I-1k.1 to I-1k.3960

I-1k

Compounds of the formula I-1k in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 11 Compounds I-1l.1 to I-1l.3960 I-1l

Compounds of the formula I-1l in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 12 Compounds I-1m.1 to I-1m.3960 I-1m

Compounds of the formula I-1m in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 13 Compounds I-1n.1 to I-1n.3960 I-1n

Compounds of the formula I-1n in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 14 Compounds I-1o.1 to I-1o.3960 I-1o

Compounds of the formula I-1o in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 15 Compounds I-1p.1 to I-1p.3960 I-1p

Compounds of the formula I-1p in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 16 Compounds I-1q.1 to I-1q.3960 I-1q

Compounds of the formula I-1q in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 17 Compounds I-1r.1 to I-1r.3960 I-1r

Compounds of the formula I-1r in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 18 Compounds I-1s.1 to I-1s.3960 I-1s

Compounds of the formula I-1s in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 19 Compounds I-1t.1 to I-1t.3960 I-1t

Compounds of the formula I-1t in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 20 Compounds I-1u.1 to I-1u.3960 I-1u

Compounds of the formula I-1u in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 21 Compounds I-1v.1 to I-1v.3960

Compounds of the formula I-1v in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 22 Compounds I-1w.1 to I-1w.3960

Compounds of the formula I-1w in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 23 Compounds I-1x.1 to I-1x.3960

Compounds of the formula I-1x in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 24 Compounds I-1y.1 to I-1y.3960

Compounds of the formula I-1y in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 25 Compounds I-1z.1 to I-1z.3960

Compounds of the formula I-1z in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 26 Compounds I-1za.1 to I-1za.3960

Compounds of the formula I-1za in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 27 Compounds I-1zb.l to I-1zb.3960

Compounds of the formula I-1zb in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

TABLE 28 Compounds I-1zc.1 to I-1zc.3960

Compounds of the formula I-1zc in which the substituents A, R¹, R² and R³ for each individual compound correspond in each case to one row of Table A.

The compound of the formula I where R⁷ is hydroxyl is prepared by reacting an activated carboxylic acid IVb or a carboxylic acid IVa, which is preferably activated in situ, with a cyclohexane-1,3-dione of the formula III to give the acylation product, followed by rearrangement.

L¹ is a nucleophilically replaceable leaving group, such as halogen, for example bromine or chlorine, hetaryl, for example imidazolyl or pyridyl, carboxylate, for example acetate or trifluoroacetate, etc.

The activated carboxylic acid Ivb can be employed directly, such as in the case of the benzoyl halides, or be generated in situ, for example using carbodiimides, such as ethyl-(3′-dimethylaminopropyl)carbodiimide, dicyclohexylcarbodiimide, triphenylphosphine/azodicarboxylic ester, 2-pyridine disulfide/triphenylphosphine, carbonyldiimidazole, etc.

If appropriate, it may be advantageous to carry out the acylation reaction in the presence of a base. Here, the reactants and the auxiliary base are advantageously employed in equimolar amounts. In some cases, it may be advantageous to employ a slight excess of the auxiliary base, for example from 1.2 to 1.5 molar equivalents, based on IVa or IVb.

Suitable auxiliary bases are tertiary alkylamines, pyridine or alkali metal carbonates. Suitable solvents are, for example, chlorinated hydrocarbons, such as methylene chloride or 1,2-dichloroethane, aromatic hydrocarbons, such as toluene, xylene or chlorobenzene, ethers, such as diethyl ether, methyl tert-butyl ether, tetrahydrofuran or dioxane, polar aprotic solvents, such as acetonitrile, dimethylformamide or dimethyl sulfoxide, or esters, such as ethyl acetate, or mixtures of these.

If the activated carboxylic acid component used is a halide, it may be advantageous to cool the reaction mixture to 0-10° C. when adding this reactant. The mixture is subsequently stirred at 20-100° C., preferably at 25-50° C., until the reaction has gone to completion. Work-up is carried out in a customary manner, for example by pouring the reaction mixture into water and extracting the product of value. Solvents which are suitable for this purpose are, in particular, methylene chloride, diethyl ether and ethyl acetate. After the organic phase has been dried and the solvent has been removed, the crude ester can be employed for the rearrangement without further purification.

The rearrangement of the esters to give the compounds of the formula I is advantageously carried out at 20-100° C. in a solvent and in the presence of a base and, if appropriate, using a cyano compound as catalyst.

Suitable solvents are, for example, acetonitrile, methylene chloride, 1,2-dichloroethane, dioxane, ethyl acetate, toluene or mixtures of these. Preferred solvents are acetonitrile and dioxane.

Suitable bases are tertiary amines, such as triethylamine, aromatic amines, such as pyridine, or alkali metal carbonates, such as sodium carbonate or potassium carbonate, which are preferably employed in an equimolar amount or an up to 4-fold excess, based on the ester. Preference is given to using triethylamine or alkali metal carbonate, preferably in twice the equimolar amount, based on the ester.

Suitable cyano compounds are inorganic cyanides, such as sodium cyanide or potassium cyanide, and organic cyano compounds, such as acetonecyanohydrin or trimethylsilyl cyanide. They are employed in an amount of 1-50 mol percent, based on the ester. Preference is given to using acetonecyanohydrin or trimethylsilyl cyanide, for example in an amount of 5-15, preferably about 10, mol percent, based on the ester.

Work-up can be carried out in a manner known per se. The reaction mixture is, for example, acidified with dilute mineral acid, such as 5% strength hydrochloric acid or sulfuric acid, and extracted with an organic solvent, for example methylene chloride or ethyl acetate. The organic extract can be extracted with 5-10% strength alkali metal carbonate solution, for example sodium carbonate or potassium carbonate solution. The aqueous phase is acidified and the precipitate that is formed is filtered off with suction and/or extracted with methylene chloride or ethyl acetate, dried and concentrated. B. Preparation of Compounds of the Formula I where R⁷=Halogen is Carried out by Reacting Cyclohexenone Derivatives of the Formula I (where R⁷=Hydroxyl) with Halogenating Agents:

Here and below, “compound Ia” is a compound of the formula I where Hex is a radical of the formula IIa and, correspondingly, compound Ib is a compound of the formula I where Hex is a radical IIb.

Suitable halogenating agents are, for example, phosgene, diphosgene, triphosgene, thionyl chloride, oxalyl chloride, phosphorus oxychloride, phosphorus pentachloride, mesyl chloride, chloromethylene-N,N-dimethylammonium chloride, oxalyl bromide, phosphorus oxybromide, etc. C. Preparation of Compounds of the Formula I where R⁷═OR¹⁴, OSO₂R¹⁵, OPOR¹⁶R¹⁷ or OPSR¹⁶R¹⁷ by Reacting Cyclohexenone Derivatives of the Formula I (where R⁷=hydroxyl) with Alkylating, Sulfonylating or Phosphonylating Agents Vα, Vβ, Vγ and Vδ, Respectively.

L² is a nucleophilically replaceable leaving group, such as halogen, for example chlorine or bromine, hetaryl, for example imidazolyl, carboxylate, for example acetate, or sulfonate, for example mesylate or triflate, etc.

Compounds of the formula Vα, Vβ, Vγor Vδ can be employed directly, such as in the case of the carbonyl halides, or be generated in situ, for example activated carboxylic acids (using carboxylic acid and dicyclohexylcarbodiimide, etc.). D. Compounds of the Formula I where R⁷=OR¹⁴, SR¹⁴, POR¹⁶R¹⁷, NR¹⁸R¹⁹, ONR¹⁸R¹⁹ or N-Bonded Heterocyclyl are Prepared by Reacting Compounds of the Formula I where R⁷=Halogen, OSO₂R¹⁵ with Compounds of the Formula VIα, VIβ, VIγ, VIδ, VIε or VIη, if Appropriate in the Presence of a Base or with Prior Formation of Salt.

E. Compounds of the Formula I where R⁷=SOR¹⁵, SO₂R¹⁵ are Prepared, for Example, by Reacting Compounds of the Formula I where R⁷=SR¹⁵ with an Oxidizing Agent.

Suitable oxidizing agents are, for example, m-chloro-perbenzoic acid, peroxyacetic acid, trifluoroperoxyacetic acid, hydrogen peroxide, if appropriate in the presence of a catalyst, such as tungstate.

For the reactions mentioned under points B to E, the following conditions apply:

The starting materials are generally employed in equimolar amounts. However, it may also be advantageous to employ an excess of one or the other component.

If appropriate, it may be advantageous to carry out the reactions in the presence of a base. Reactants and base are advantageously employed in equimolar amounts.

With respect to the processes C and D, it may, in certain cases, be advantageous to employ an excess of base, for example 1.5 to 3 molar equivalents, in each case based on the starting material.

Suitable bases are tertiary alkylamines, such as triethylamine, aromatic amines, such as pyridine, alkali metal carbonates, for example sodium carbonate or potassium carbonate, alkali metal bicarbonates, such as sodium bicarbonate and potassium bicarbonate, alkali metal alkoxides, such as sodium methoxide, sodium ethoxide, potassium tert-butoxide, or alkali metal hydrides, for example sodium hydride. Preference is given to using triethylamine or pyridine.

Suitable solvents are, for example, chlorinated hydrocarbons, such as methylene chloride or 1,2-dichloroethane, aromatic hydrocarbons, for example toluene, xylene or chlorobenzene, ethers, such as diethyl ether, methyl tert-butyl ether, tetrahydrofuran or dioxane, polar aprotic solvents, such as acetonitrile, dimethylformamide or dimethyl sulfoxide, or esters, such as ethyl acetate, or mixtures of these.

In general, the reaction temperature is in the range from 0° C. to the boiling point of the reaction mixture.

Work-up can be carried out in a manner known per se to give the product.

Depending on the reaction conditions, in the processes B to D the compounds Ia, Ib, or mixtures of these can be formed. The latter can be separated by classic separation methods, for example crystallization, chromatography, etc.

The cyclohexanediones of the formula III used as starting materials are known or can be prepared by processes known per se (e.g. EP-A 71 707, EP-A 142 741, EP-A 243 313, U.S. Pat. No. 4,249,937, WO 92/13821).

The alkylating agents Vα, sulfonylating agents Vβ, phosphonylating agents Vγ and Vδ, and the compounds VIα, VIβ, VIγ, VIδ and VIε are likewise known, or they can be prepared by known processes.

The carboxylic acids of the formula IVa and their activated derivatives IVb are novel and also form part of the subject-matter of the present invention.

Scheme 1 shows a general route to compounds of the formula IVa in which A is oxygen or NR⁶.

According to scheme 1, benzazolonecarboxylic acids of the formula IVa (A=O or NR⁶) can be prepared from 2-nitroanilines or 2-nitrophenols of the formula VIII, which are substituted in position 3. In step a), the nitro compounds VIII are initially brominated in the position meta to the nitro group. Brominating agents which are customary for this purpose are bromine, N-bromosuccinimide, N-bromohydantoin or pyridinium perbromide which, if appropriate, are employed together with a Lewis acid such as FeBr₃. The bromination is usually carried out in an inert solvent. Suitable solvents are aliphatic or cycloaliphatic hydrocarbons, for example n-hexane or cyclohexane, halogenated hydrocarbons, for example dichloromethane, trichloromethane, carbon tetrachloride, trichloroethane, trichloroethylene, heteroaromatic compounds, such as pyridine, or anhydrous inorganic or organic acids, such as acetic acid. Customary reaction temperatures are in the range from −15° C. to 150° C., preferably in the range from −15° C. to 100° C. Methods for brominating nitro compounds are known, for example from Organikum, 16th ed., 1986, p. 315.

Subsequently, in step b), the nitro group of the compound IX is reduced to the amino group. Suitable reducing agents are, for example, hydrazines, metal hydrides, such as aluminum hydride, and complex hydrides derived therefrom, such as lithium aluminum hydride, diisobutyl aluminum hydride, or boranes, and also nascent hydrogen, for example iron, zinc or tin the presence of acids, such as hydrochloric acid or carboxylic acids, such as acetic acid. A further suitable reducing agent is hydrogen in the presence of catalytic amounts of transition metals such as nickel, palladium, platinum, ruthenium or rhodium. The transition metals can be used as such or in supported form, for example on activated carbon, in the form of activated metals, for example, Raney nickel, or in the form of soluble complex compounds. The reaction is preferably carried out in a solvent. Suitable solvents for the reduction are, depending on the solubility of the substrate to be hydrogenated and the chosen reducing agent, for example C₁-C₄-alcohols, such as methanol, ethanol, n-propanol, isopropanol or n-butanol, halogenated C₁-C₆-hydrocarbons, such as dichloromethane, trichloromethane, trichloroethane, trichloroethylene, aromatic hydrocarbons, such as benzene, toluene, xylenes, chlorobenzene, aqueous solutions of inorganic acids, such as aqueous hydrochloric acid, or organic acids, and mixtures thereof with water. The reduction is usually carried out at temperatures in the range from −15° C. to +100° C., preferably in the range from 0° C. to 40° C. The reduction with hydrogen is usually carried out at a hydrogen pressure in the range from 1 to 50 bar. Catalytic hydrogenations with hydrogen are preferably carried out in the range from 1 to 10 bar. For the catalytic hydrogenation of aromatic nitro groups, see, for example, Rylander in “Catalytic Hydrogenation over Platinum Metals”, Academic Press, New York, 1967, 168-202; Furst et al., Chem. Rev. 65 (1965), 52; Tepko et al., J. Org. Chem. 45 (1980), 4992.

The 3-bromoaniline X is then, in step c), condensed to the heterocycle by reacting the compound X with a carbonic acid equivalent, such as methyl chloroformate, phosgene or its synthesis equivalents, such as diphosgene or triphosgene, under conditions which are customary for phosgenation. In general, the cyclization is carried out under neutral to acidic reaction conditions at temperatures in the range from 0° C. to 150° C. and preferably in the range from 20° C. to 120° C. The phosgenation is usually carried out in a solvent. Suitable solvents are, in particular, aliphatic or cycloaliphatic hydrocarbons, such as n-hexane or cyclohexane, halogenated hydrocarbons, such as dichloromethane, chloroform, trichloroethane, trichloroethylene, aromatic hydrocarbons, such as benzene, aliphatic ethers, such as diethyl ether, methyl tert-butyl ether, or cyclic ethers, such as tetrahydrofuran or dioxane. Phosgenation methods are known, see, for example, Justus Liebigs Ann. Chem., (2), 1978 193-213; J. Med. Chem., 30 (N 7) (1987), 1166-1176, J. Heterocycl. Chem. 28 (8) (1991), 1937-1939; J. Nat. Prod. 58 (3) (1995), 456-458.

In step d), the substituent R² is introduced, for example, by reacting the 5-bromobenzazol-2-one XI obtained in step c) with R²-L or its precursor, L being a nucleophilically displaceable leaving group. Suitable leaving groups are, for example, halogen, such as chlorine, bromine or iodine, carboxylate, such as acetate or trifluoroacetate, or sulfonates, such as tosylate, mesylate or triflate. The reaction is preferably carried out in the presence of an auxiliary base, for example alkali metal carbonates or alkaline earth metal carbonates, such as sodium carbonate, potassium carbonate, magnesium carbonate or calcium carbonate, alkali metal hydrides or alkaline earth metal hydrides, for example sodium hydride, tertiary alkylamines, for example triethylamine, aromatic amines, for example pyridine, DMPU. The reaction is generally carried out at temperatures in the range from −15° C. to 150° C. and preferably at from 0° C. to 100° C. The reaction is usually carried out in a solvent. Suitable solvents are, for example, the abovementioned inert hydrocarbons, the abovementioned halogenated hydrocarbons, aromatic hydrocarbons, such as benzene, toluene, xylene or chlorobenzene, the abovementioned acyclic or cyclic ethers, furthermore polar aprotic solvents, such as dimethylformamide, acetonitrile or dimethyl sulfoxide. Methods for introducing a substituent at a heterocylic amide nitrogen atom are known, see also Eur. J. Med. Chem. 30 (9) (1995), 715-719; Tetrahedron 54 (9) (1998), 1763-1772.

Successive reaction of XII with magnesium or alkylmagnesium halides to the corresponding Grignard reagent and subsequent reaction of the Grignard reagent with carbon dioxide gives the carboxylic acid IVa (step e)). Customary reaction temperatures are in the range from −15° C. to 150° C., preferably in the range from −15° C. to 100° C. Suitable solvents are anhydrous solvents, in particular the abovementioned inert cyclic or acyclic hydrocarbons, the abovementioned aromatic hydrocarbons or the abovementioned acyclic or cyclic ethers. The benzazolone-5-carboxylic acid IVa is obtained by introducing dry carbon dioxide into the resulting solution of the Grignard reagent corresponding to XII and subsequent aqueous work-up. The carbon dioxide pressure is usually from 1 to 6 bar.

Alternatively, XII can be converted into carboxylic acid IVa by halogen-metal exchange using an alkali metal alkyl, for example a lithium alkyl, such as methyllithium, n-butyllithium or tert-butyllithium, and subsequent reaction of the lithiated product with CO₂. Customary reaction temperatures are in the range from −100° C. to 0° C., preferably in the range from −78° C. to −50° C. Suitable solvents are anhydrous solvents, in particular the abovementioned inert hydrocarbons, the abovementioned aromatic hydrocarbons or the abovementioned acyclic or cyclic ethers. Introduction of dry carbon dioxide into the solution of the lithiated product of XII gives the benzazolonecarboxylic acid IVa. The carbon dioxide pressure is usually from 1 to 6 bar.

Reaction step e) in scheme 1 can also be realized by reacting XII with carbon monoxide, a base and water, under elevated pressure in the presence of a palladium, nickel, cobalt or rhodium catalyst.

The catalysts nickel, cobalt, rhodium and in particular palladium can be present in metallic form or in the form of customary salts, such as in the form of halogen compounds, for example palladium(II) chloride, rhodium(III) chloride hydrate, acetates, for example palladium(II) acetate, cyanides, etc., in the known valence states. Metal complexes with tertiary phosphines, metal alkyl carbonyls, metal carbonyls, for example CO₂(CO)₈, Ni(CO)₄, metal carbonyl complexes with tertiary phosphines, for example (PPh₃)₂Ni(CO)₂, or transition metal salts complexed with tertiary phosphines can also be employed. The lastmentioned embodiment is preferred, in particular when the catalyst used is palladium. Here, the type of phosphine ligands is of minor importance. Suitable ligands are, for example, those of the formula:

where the radicals R²⁴ to R²⁶ are low-molecular-weight alkyl, for example C₁-C₆-alkyl, aryl, C₁-C₄-alkylaryl, for example benzyl, phenethyl, or aryloxy. Aryl is, for example naphthyl, anthryl and preferably unsubstituted or substituted phenyl, where, with respect to the substituents, attention has to be paid only to their inertness to the carboxylation reaction, otherwise they can be varied widely and include all inert organocarbon radicals, such as C₁-C₆-alkyl radicals, for example methyl, carboxyl radicals, such as COOH, COOM (M is, for example, an alkali metal, alkaline earth metal or ammonium salt), or organocarbon radicals attached via oxygen, such as C₁-C₆-alkoxy radicals. A is a divalent organic radical, for example C₁-C₄-alkylene, 1,2-cycloalkylene, α,α′-ferrocenediyl, α,α-biphenyl or similar bifunctional groups.

The phosphine complexes can be prepared in a manner known per se, for example as described in the documents mentioned at the outset. For example, customary commercially available metal salts such as palladium(II) chloride or palladium(II) acetate are used as starting materials and the phosphine, for example P(C₆H₅)₃, P(n-C₄H₉)₃, PCH₃(C₆H₅)₂, 1,2-bis(diphenylphosphino)ethane, is added.

The amount of phosphine, based on the transition metal, is usually from 0 to 20, in particular from 0.1 to 10, molar equivalents, particularly preferably from 1 to 5 molar equivalents.

The amount of transition metal is not critical. Of course, for reasons of cost, preference is given to using a relatively small amount, for example from 0.1 to 10 mol %, in particular from 1 to 5 mol %, based on the starting material IVa.

For preparing the benzazolonecarboxylic acid IVa, the reaction is carried out with carbon monoxide and at least equimolar amounts of water, based on the bromide obtained in step d). The reaction component water can simultaneously also serve as solvent, i.e. the maximum amount is not critical.

However, depending on the nature of the starting materials and the catalysts used, it may also be advantageous for the solvent used to be, instead of the reaction component, another inert solvent or the base which is used for the carboxylation.

Suitable inert solvents for carboxylation reactions are customary solvents such as hydrocarbons, for example toluene, xylene, hexane, pentane, cyclohexane, ethers, for example methyl tert-butyl ether, tetrahydrofuran, dioxane, dimethoxyethane, substituted amides, such as dimethylformamide, persubstituted ureas, such as tetra-C₁-C₄-alkylureas, or nitrites, such as benzonitrile or acetonitrile.

In a preferred embodiment of the process, one of the reaction components, in particular the base, is used in an excess, so that no additional solvent is necessary.

Bases which are suitable for the process are all inert bases which are able to bind hydrogen iodide or hydrogen bromide liberated during the reaction. Examples which may be mentioned here are tertiary amines, such as tert-alkylamines, trialkylamines, such as triethylamine, cyclic amines, such as N-methylpiperidine or N,N′-dimethylpiperazine, pyridine, alkali metal carbonates or bicarbonates, or tetraalkyl-substituted urea derivatives, such as tetra-C₁-C₄-alkylurea, for example tetramethylurea.

The amount of base is not critical: customarily from 1 to 10, in particular from 1 to 5, mol are used. When the base is simultaneously used as solvent, the amount is generally such that the reaction components are dissolved, unnecessarily high excesses being avoided for reasons of practicability in order to save costs, to be able to employ small reaction vessels and to ensure that the reaction components have maximum contact.

During the reaction, the carbon monoxide pressure is adjusted such that an excess of CO, based on the bromide, is always present. At room temperature, the carbon monoxide pressure is preferably from 1 to 250 bar, in particular from 5 to 150 bar, of CO.

The carbonylation is generally carried out continuously or batchwise at from 20 to 250° C., in particular from 30 to 150° C. In the case of batchwise operation, carbon monoxide is advantageously continuously injected onto the reaction mixture to maintain a constant pressure.

It is, of course, also possible to carry out reaction step e) first and then reaction step d).

The 2-nitroanilines or 2-nitrophenols of the formula VIII, which are substituted in the 3-position, used as starting materials for the synthesis of the benzazolonecarboxylic acids IVa are known and can be prepared by processes known per se. Alternatively, the compounds IX in which A is oxygen can be prepared in the manner shown below in scheme 7.

A further general route to the benzazolonecarboxylic acids of the formula IVa is shown in scheme 2.

Starting with the 2-nitroanilines or 2-nitrophenols of the formula VIII, which are substituted in the 3-position, the substituted acetophenone XIII can be prepared by Friedel-Crafts acylation in step f). The acetyl group can be introduced in a known manner by reacting the compound VIII with acetic acid or activated acetic acid, such as acetic anhydride or acetyl chloride, in the presence of a Lewis acid such as aluminum trichloride, boron trichloride or trifluoroacetic acid, under anhydrous conditions. Usually, more than 1 mol of Lewis acid is required per mole of ketone formed, since the ketone formed binds the Lewis acid as a complex. After the reaction has ended, this complex is cleaved hydrolytically. Friedel-Crafts acylations are usually carried out in a solvent. Suitable solvents are the abovementioned cyclic and acyclic hydrocarbons, the abovementioned halogenated hydrocarbons, aromatic hydrocarbons, such as nitrobenzene, or the abovementioned ethers. The reaction temperatures are generally in the range from 0° C. to 150° C. and preferably in the range from 20° C. to 120° C. Methods for introducing acyl groups are known, see, for example, Organikum, 16th ed. 1986, p. 325.

In step g), the substituted acetophenone XIII is then reduced to the amino compound XIV. The reduction is carried out in the manner described in step b) in scheme 1. In step h), the aniline derivative XIV is then phosgenated in the manner described in step c) in scheme 1. The substituent R² can be introduced similarly to step d) in scheme 1 (step i) in scheme 2).

The compound XVI obtained in step i) in scheme 2 is converted into the benzazolonecarboxylic acid IVa with the aid of the haloform reaction. To this end, a halogenating agent, such as hypohalite, for example hypochlorite, or chlorine in alkaline solution is allowed to act on the compound XVI. Initially, a trihalomethylcarbonyl derivative is formed, which, under the alkaline reaction conditions, is cleaved hydrolytically with formation of the desired benzazolonecarboxylic acid IVa. Suitable bases are, in particular, alkali metal hydroxides, such as sodium hydroxide or potassium hydroxide. The reaction is usually carried out in solution. Suitable solvents are in particular water, mixtures of water and organic solvents, such as C₁-C₄-alcohols, for example methanol, ethanol, propanol, butanol, or the abovementioned ethers. Customary reaction temperatures are in the range from 0° C. to 150° C., preferably in the range from 20° C. to 120° C. For the haloform reaction, see, for example, Organikum, 16th ed. 1986, p. 375.

If A in formula IVa is sulfur, the benzazolonecarboxylic acids of the general formula IVa can also be prepared in the manner shown in scheme 3.

According to scheme 3, the benzazolonecarboxylic acids of the formula IVa where A=sulfur can be prepared from the aminobenzothiazoles XVII. The 2-aminobenzothiazole XVII is converted into the 2-halobenzothiazole compound XVIII in a manner known per se under Sandmeyer conditions (step k)). In this manner, further functionalities can be introduced in the 2-position of the benzothiazole ring.

To this end, the 2-aminobenzothiazole XVII is initially reacted with inorganic or organic nitrite, such as sodium nitrite in the presence of acid, such as hydrochloric acid, or with tert-butyl nitrite. The resulting diazonium salt is then reacted with an inorganic halide, such as sodium chloride, with addition of copper or a Cu(I) halide, such as Cu(I) chloride. The reaction is generally carried out at temperatures in the range from 0° C. to 150° C. and preferably in the range from 20° C. to 100° C. Suitable solvents are in particular water or mixtures of water with organic solvents, such as the abovementioned alcohols or ethers. For preparing aromatic halides, in particular chlorides, according to Sandmeyer, see also Organikum, 16th ed. 1986, p. 545.

In step 1), the 2-halobenzothiazole compound XVIII can then be hydrolyzed under acidic or alkaline conditions to give the benzothiazolone. To this end, the compound XVIII is treated with a base, such as alkali metal hydroxide or alkaline earth metal hydroxide, for example sodium hydroxide, potassium hydroxide or magnesium hydroxide, or alkali metal alkoxide, such as sodium ethoxide or potassium methoxide, or with an acid, such as hydrochloric acid. The hydrolysis is usually carried out in a solvent. Suitable solvents are, depending on the base used, polar aprotic solvents, such as dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone or acetonitrile, ethers, such as tetrahydrofuran or dioxane, water and mixtures of water with the abovementioned alcohols, ethers or polar aprotic solvents. The hydrolysis is generally carried out at from 0° C. to 150° C. and preferably at from 20° C. to 120° C. For the hydrolysis of haloheteroaromatic compounds to keto compounds see also J. Med. Chem. 20 (No. 6) (1977), 791-796.

In step m), the substituent R² is introduced into the compound XIX as described in step d) in scheme 1. For the hydrolysis in step n), for example, the benzazolone methyl ester XX obtained in step m) is reacted with alkali metal hydroxide, for example lithium hydroxide, sodium hydroxide or potassium hydroxide, with alkaline earth metal hydroxide, such as magnesium hydroxide, or with alkali metal iodides, such as sodium iodide, in a suitable solvent, preferably in the absence of oxygen. Usual reaction temperatures are in the range from 0° C. to 200° C. and in particular in the range from 20° C. to 180° C. Suitable solvents are the abovementioned aliphatic or cycloaliphatic hydrocarbons, the halogenated hydrocarbons, the aromatic hydrocarbons, the abovementioned ethers and alcohols, aqueous monophasic systems, and also pyridine. For hydrolysis, see, for example, Organikum, 16th ed. 1986, p. 415, McMurry, Org. React. 24 (1976), 187; Taschner et al., Rocz. Chem. 30 (1956), 323; Houben-Weyl: “Methoden der organischen Chemie” [Methods of Organic Chemistry], volume E 8 b 1994; p. 1010 f.; J.Chem. Soc. Perkin Trans. 1, No. 12 (1976), 1291-1296; in particular A. R. Katritzky et al., J. Heterocycl. Chem., 30 (1) (1993) 135-139. The synthesis of the starting material XVII is described in PCT/EP 00/04042 and PCT/EP 00/04040.

A further route to the compounds of the formula IVa is shown in scheme 4.

In step o), the 2-chlorobenzothiazole compounds XXII can be prepared in a Sandmeyer reaction from the 2-aminobenzothiazoles of the formula XXI, which are known per se. The reaction conditions required correspond to those for step k) in scheme 3. The 2-chlorobenzothiazole XXII can be brominated in a manner similar to that of step a) in scheme 1, the bromine substituent being introduced selectively in the position ortho to R¹ (step p)). The compound XXIII is then, under the conditions given for step 1) in scheme 3, subjected to basic hydrolysis (step q)). In step r), the substituent R² can be introduced into XXIV under the conditions described for step d) in scheme 1. The carboxyl group is introduced (step s)) according to the reaction conditions described in step e) in scheme 1.

A variant for preparing the benzothiazolonecarboxylic acid IVa (A=S) is shown in scheme 5.

Again, the initial starting materials are substituted 2-aminobenzothiazoles XXI which are converted in the manner described above into the 2-chlorobenzothiazoles XXII (step o), see scheme 3). In step u), the 2-chlorobenzothiazoles XXII are then subjected to a Friedel-Crafts acylation under the conditions given in step f) in scheme 2, giving the compound XXVII. XXVII is hydrolyzed in a manner similar to that described for reaction step q) in scheme 4. In step w), the substituent R² is introduced into XXVIII in a manner known per se, for example as described in step d) in scheme 1. The substituted acetophenone XXIX is then, in the concluding haloform reaction in step x), under the conditions given in step j) in scheme 2, converted into the desired benzazolonecarboxylic acid IVa, with loss of a carbon.

A further route to benzazolonecarboxylic acids of the formula IVa (A=sulfur) is shown in scheme 6.

The o-chloronitrobenzenes of the formula XXX, which are known per se, are initially converted with alkali metal salts of benzyl ercaptan into the corresponding thioethers XXXI (step 1)). The substitution is usually carried out in one of the abovementioned aliphatic or cycloaliphatic hydrocarbons, halogenated hydrocarbons, aromatic hydrocarbons, ethers, in dimethylformamide, NMP, sulfolane or dimethyl sulfoxide. Customary reaction temperatures are in the range from 0° C. to 250° C. and preferably in the range from 50° C. to 175° C. Methods for nucleophilic substitution are known, see also A. Bagno et al., J. Chem. Soc. Perkin Trans. II, 1991 (5), 651-655; J. R. Beck et al., J. Org. Chem. 43 (10), (1978), 2048-2052.

In step 2), the compound XXXI is then reduced to amino compound XXXII. The required reaction conditions correspond to those for step b) in scheme 1. The amino compound XXXII is then cyclized under the reaction conditions described in step c) in scheme 1 using carbonic acid equivalents, to give the benzothiazolone XXXIII (step 3)). The substituent R² is subsequently introduced under the reaction conditions described in step d) in scheme 1 (step 4)). The acetyl group is introduced in the position ortho to substituent R¹ by Friedel-Crafts acylation of the compound XXXIV (step 5)). The required reaction conditions correspond to those of step f) in scheme 2. The desired benzazolonecarboxylic acid IVa can be obtained from compound XXXV by haloform reaction (step 6)). The required reaction conditions correspond to those in step j) in scheme 2.

In a similar manner as in scheme 1, compounds of the formula IVa where A=sulfur can be obtained in a variant of this process starting with o-chloronitrobenzenes XXX by initially brominating the thioether XXXI obtained in step 1). The required reaction conditions correspond to those of step a) in scheme 1. The subsequent reduction of the nitro group to the amino group is carried out under the conditions mentioned in step b) in scheme 1. Condensation with carbonic acid equivalents gives the benzothiazolones. The required reaction conditions correspond to those of step c) in scheme 1. The substituent R² is introduced in the customary manner, analogously to step d) in scheme 1. The carboxyl group is introduced by the procedure described in step e) in scheme 1.

A further route to benzazolonecarboxylic acids where A=oxygen is shown in scheme 7.

According to scheme 7, for example, o-chloronitrobenzenes of the formula XXX can be converted with alkali metal salts of alkoxides into the corresponding o-nitroethers XXXVI (step 7)). This nucleophilic substitution on the aromatic ring is generally carried out with exclusion of water, usually in a solvent. Suitable solvents are, in particular, the abovementioned aliphatic or cycloaliphatic hydrocarbons, halogenated hydrocarbons, aromatic hydrocarbons, ethers, DMF, NMP, sulfolane or dimethyl sulfoxide. The required reaction temperatures are generally in the range from 0° C. to 250° C. and preferably from 50° C. to 175° C. Methods for preparing aromatic ethers from o-nitrochloro compounds are known, see also A. Bagno et al., J.Chem. Soc. Perkin Trans. II, 1991 (5), 651-655; J. R. Beck et al., J. Org. Chem. 43 (10) (1978), 2048-2052.

The resulting o-nitroanisole XXXVI is brominated under the reaction conditions given in step a) in scheme 1, the bromine atom being introduced selectively in position para to the methoxy group (step 8)).

In step 9), the hydroxyl group is then exposed by ether cleavage under acidic reaction conditions in the presence of a Lewis acid, such as aluminum trichloride, aluminum tribromide or hydrohalic acids, such as hydriodic acid or hydrobromic acid, giving 4-bromo-2-nitrophenols of the formula IX. The ether cleavage is usually carried out in a solvent. Suitable solvents are the abovementioned acyclic and cyclic hydrocarbons, halogenated hydrocarbons, aromatic hydrocarbons or acids, such as acetic acid. The ether cleavage is generally carried out at temperatures in the range from −15° C. to 150° C., preferably in the range from 0° C. to 100° C. For the cleavage of phenol ethers, see also Organikum, 16th ed. 1986, p. 192.

The further reaction steps 10) to 13) in scheme 7 correspond to reaction steps b) to e) in scheme 1.

The examples below serve to illustrate the invention.

EXAMPLE 1 Preparation of 3,4-dimethyl-5-(1′,3′-cyclohexanedion-2′-yl)carbonylbenzothiazol-2-one (Compound I-1a.1129)

1.1 Methyl 2-chloro-4-methylbenzothiazole-5-carboxylate

A solution of 5 g (22.5 mmol) of methyl 2-amino-4-methyl-benzothiazole-5-carboxylate in 2 l of acetonitrile was admixed with 10 ml of water, 4.5 g (44.8 mmol) of copper(I) chloride, 6.6 g of sodium chloride (110 mmol) and 2 ml of 15-crown-5. A solution of 3 g (29 mmol) of tert-butyl nitrite was then added dropwise with stirring, the solution was heated at reflux for 15 h, the resulting precipitate was filtered off and the solution was concentrated under reduced pressure. The residue was then extracted three times with in each case 500 ml of ethyl acetate. To this end, the solvent was heated to boiling point and the solution was filtered whilst hot. The extracts were concentrated under reduced pressure. The residue was purified by trituration with n-hexane/diethyl ether. This gave 4.2 g (17.4 mmol, 77% yield) of methyl 2-chloro-4-methylbenzothiazole-5-carboxylate of m.p. 112° C.

¹H-NMR (CDCl₃): δ (ppm)=2.98 (s, 3H), 3.94 (s, 3H), 7.64 (d, 1H), 7.95 (d, 1H).

1.2 Methyl 4-methylbenzothiazol-2-one-5-carboxylate

A solution of 22.5 g (93 mmol) of methyl 2-chloro-4-methyl-benzothiazole-5-carboxylate in 360 ml of N-methylpyrrolidone was admixed with 13.6 g (186 mmol) of potassium methoxide and heated at 100° C. for 5 hours. After cooling, the resulting precipitate was filtered off with suction and the filtrate was admixed with water. The pH of the reaction solution was then adjusted to pH 1, the aqueous solution was extracted three times with ethyl acetate and the combined organic phases were washed and dried. The solvent was removed under reduced pressure and the residue was purified by trituration with methylene chloride/n-hexane. This gave, in a yield of 55%, 11.38 g (51 mmol) of methyl 4-methylbenzothiazol-2-one-5-carboxylate of m.p. 262° C.-266° C.

¹H-NMR (CDCl₃): δ (ppm)=2.64 (s, 3H), 3.91 (s, 3H), 7.28 (d, 1H), 7.74 (d, 1H), 9.94 (br s, 1H, NH).

1.3 Methyl 3,4-dimethylbenzothiazol-2-one-5-carboxylate

A solution of 11.38 g (51 mmol) of methyl 4-methylbenzo-thiazol-2-one-5-carboxylate in 400 ml of acetone was admixed with 14.18 g of potassium carbonate. 5.1 ml (54 mmol) of dimethyl sulfate were then added dropwise with stirring, and the mixture was stirred at 23° C. for 78 hours. The precipitated solid was filtered off and the solvent was removed under reduced pressure. Recrystallization from ether gave, in a yield of 84%, 10.15 g (43 mmol) of methyl 3,4-dimethylbenzothiazol-2-one-5-carboxylate of m.p. 97° C.-100° C.

¹H-NMR (CDCl₃): δ (ppm)=2.78 (s, 3H), 3.77 (s, 3H), 3.92 (s, 3H), 7.28 (d, 1H), 7.36 (d, 1H).

1.4 Methyl 3,4-dimethylbenzothiazol-2-one-5-carboxylic acid

A solution of 10.15 g (43 mmol) of methyl 3,4-dimethylbenzo-thiazol-2-one-5-carboxylate in 100 ml of tetrahydrofuran and 100 ml of water was admixed with 2.06 g (86 mmol) of lithium hydroxide. The solution was then heated at reflux for 2 hours. After cooling, the tetrahydrofuran was removed under reduced pressure, the remaining aqueous solution was acidified and the precipitated solid was filtered off with suction and dried. More product was obtained by extracting the mother liquor with ethyl acetate. This gave a total of 8 g (36 mmol, 83% yield) of 3,4-dimethylbenzothiazol-2-one-5-carboxylic acid of m.p. 235° C.-239° C.

¹H-NMR (DMSO-D₆): δ (ppm)=2.77 (s, 3H), 3.66 (s, 3H), 7.42 (d, 1H), 7.56 (d, 1H).

1.5 Cyclohexenon-3-yl 3,4-dimethylbenzothiazol-2-one-5-carboxylate

1.1 g (5 mmol) of 3,4-dimethylbenzothiazol-2-one-5-carboxylic acid, 0.58 g of 1,3-cyclohexanedione and 1.25 g of ethyl(3′-dimethylaminopropyl)carbodiimide were dissolved in 40 ml of acetonitrile, and the solution was stirred at 50° C. for 4 hours. After the reaction had ended, the precipitate was filtered off and the solution was concentrated. The residue was taken up in water and extracted with methylene chloride. The organic phase was washed and dried and the solvent was then removed. Chromatography of the residue on silica gel (mobile phase: cyclohexane/ethyl acetate, gradient from 100:0 to 50:50) gave 0.77 g (2.4 mmol, 48% yield) of cyclohexenone-3-yl 3,4-dimethylbenzothiazol-2-one-5-carboxylate of m.p. 144° C.-146° C.

¹H-NMR (CDCl₃): δ (ppm)=1.18 (s, 6H), 2.37 (s, 2H), 2.57 (s, 2H), 2.86 (s, 3H), 3.81 (s, 3H), 6.05 (s, 1H), 7.37 (d, 1H), 7.68 (d, 1H).

1.6 3,4-Dimethyl-5-(1′,3′-cyclohexanedion-2′-yl)carbonyl-benzothiazol-2-one

With stirring, 0.97 g of potassium carbonate and a drop of trimethylsilyl cyanide were added to a solution of 0.43 g (1.4 mmol) of cyclohexenon-3-yl 3,4-dimethyl-benzothiazol-2-one-5-carboxylate in 40 ml of acetonitrile. The reaction mixture was heated at 45° C. for 16 hours, the precipitated solid was filtered off, the solvent was removed under reduced pressure and the residue was then taken up in water. The aqueous phase was adjusted to pH 7 and extracted with methylene chloride. The solvent was removed, giving 0.09 g (0.3 mmol, 20% yield) of 3,4-dimethyl-5-(1′,3′-cyclohexanedion-2′-yl)carbonylbenzo-thiazol-2-one as an oil.

¹H-NMR: δ (ppm)=7.31 (d), 6.86 (d), 3.80 (s), 2.83 (m), 2.60 (s), 2.47 (m), 2.10 (m).

EXAMPLE 2 Preparation of 3,4-dimethyl-5-(5′,5′-dimethyl-1′,3′-cyclohexanedion-2′-yl)-carbonylbenzothiazol-2-one (Compound I-1c.1129)

2.1 5′,5′-Dimethylcyclohexenone-3′-yl 3,4-dimethylbenzothiazol-2-one-5-carboxylate

The reaction was carried out similarly to the procedure described in Example 1.5 using, instead of 0.58 g of 1,3-cyclohexanedione, 0.72 g of 5,5-dimethyl-1,3-cyclo-hexanedione.

0.66 g (1.9 mmol, 39% yield) of 5,5-dimethylcyclohexenon-3-yl 3,4-dimethylbenzothiazol-2-one-5-carboxylate of m.p. 123°-126° C. was isolated.

¹H-NMR (CDCl₃): δ (ppm)=1.18 (s, 6H), 2.37 (s, 2H), 2.57 (s, 2H), 2.86 (s, 3H), 3.81 (s, 3H), 6.05 (s, 1H), 7.37 (d,1H), 7.68 (d, 1H).

2.2 3,4-Dimethyl-5-(5′,5′-dimethyl-1′,3′-cyclohexanedion-2′-yl)-carbonylbenzothiazol-2-one

The reaction was carried out similarly to the procedure described in Example 1.6 using, instead of 0.43 g (1.4 mmol) of cyclohexenon-3-yl 3,4-dimethylbenzothiazol-2-one-5-carboxylate, 0.63 g (1.8 mmol) of 5,5-dimethylcyclohexenon-3-yl 3,4-dimethylbenzothiazol-2-one-5-carboxylate and using 1.24 g of potassium carbonate instead of 0.97 g of potassium carbonate.

0.35 g (1 mmol, 56% yield) of the title compound of m.p. 173° C.-176° C. was isolated.

¹H-NMR (CDCl₃): δ (ppm)=1.14 (s, 6H), 2.32 (s, 2H), 2.56 (s, 3H), 2.68 (s, 2H), 3.79 (s, 3H), 6.82 (d, 1H), 7.27 (d, 1H), 17.60 (s, 1H).

EXAMPLE 3 Preparation of 3,4-dimethyl-5-(4′,4′,6′,6′-tetramethyl-1′,3′,5′-cyclohexane-trion-2′-yl)-carbonylbenzothiazol-2-one (Compound I-1d.1129)

3.1 4′,4′,6′,6′-Tetramethylcyclohexene-1′,5′-dion-3′-yl 3,4-dimethylbenzothiazol-2-one-5-carboxylate

The reaction was carried out similarly to the procedure described in Example 1.5 using, instead of 0.58 g of 1,3-cyclohexanedione, 0.94 g of 4,4,6,6-tetramethyl-1,3,5-cyclohexanetrione.

0.96 g (2.5 mmol, 50% yield) of 4,4,6,6-tetramethylcyclo-hexene-1,5-dion-3-yl 3,4-dimethylbenzothiazol-2-one-5-carboxylate of m.p. 145° C.-147° C. was isolated.

¹H-NMR (CDCl₃): δ (ppm)=1.40 (s, 6H), 1.48 (s, 6H), 2.86 (s, 3H), 3.82 (s, 3H), 6.28 (s, 1H), 7.39 (d, 1H), 7.72 (d, 1H).

3.2 3,4-Dimethyl-5-(4′,4′,6′,6′-tetramethyl-1′,3′,5′-cyclohexanetrion-2′-yl)-carbonylbenzothiazol-2-one

The reaction was carried out similarly to the procedure described in Example 1.6 using, instead of 0.43 g (1.4 mmol) of cyclohexenon-3-yl 3,4-dimethylbenzothiazol-2-one-5-carboxylate, 0.78 g (2 mmol) of 4,4,6,6-tetramethylcyclo-hexene-1,5-dion-3-yl 3,4-dimethylbenzothiazol-2-one-5-carboxylate and 1.24 g of potassium carbonate instead of 0.97 g of potassium carbonate.

This gave 0.17 g (0.4 mmol, 22% yield) of the title compound of m.p. 203° C. to 204° C.

¹H-NMR: δ (ppm)=7.28 (d), 6.84 (d), 3.80 (s), 2.62 (s), 1.56 (s), 1.36 (s).

In a similar manner, the compounds I of Examples 4 to 40 were prepared by reacting the respective carboxylic acid IV in a similar manner with the respective cyclohexane-1,3-dione, where in the preparation of the compounds I of Examples 20, 21 and 28 the triketone that was originally obtained was derivatized by reacting successively with oxazolyl chloride and then with pyrazole.

Ex. Structure/compound number m.p. or ¹H-NMR 1

δ (ppm) = 7.31 (d), 6.86 (d), 3.80 (s), 2.83 (m), 2.60 (s), 2.47 (m), 2.10 (m). 2

m.p. 173° C.-176° C. 3

δ (ppm) = 7.28 (d), 6.84 (d), 3.80 (s), 2.62 (s), 1.56 (s), 1.36 (s) 4

m.p. 101° C.-110° C. 5

m.p. 143° C.-150° C. 6

m.p. 207° C.-209° C. 7

m.p. 139° C.-143° C. 8

δ (ppm) = 7.12 (d), 6.82 (d), 6.00 (m), 5.30 8d), 5.17 (d), 4.63 (m), 2.68 (s), 2.33 8s), 2.29 (s), 1.12 (s) 9

m.p. 128° -130° C. 10

m.p. 115° C.-116° C. 11

δ (ppm) = 2.05 (m, 2H), 2.35 (s, 3H), 2.75 (m, 2H), 4.65 (d, 2H), 5.20 (m, 2H), 5.95 (m, 1H), 6.85 (d, 1H), 7.05 (d, 1H), 17.5 (s, 1H) 12

m.p. 150° C.-153° C. 13

δ (ppm) = 1.13 (s, 6H), 1.35 (t, 3H), 2.40 (s, 3H), 2.50 (s, 4H), 4.05 (m, 2H), 6.80 (m, 2H), 7.05 (d, 2H), 17 (s, 1H) 14

δ (ppm) = 0.95 (t, 3H), 1.40 (m, 2H), 1.65-2.30 (m, 8H), 2.45 (s, 3H), 2.90 (M, 1H), 3.15 (m, 1H), 4.15 (m, 2H), 6.85 (d, 1H), 7.25 (d, 1H), 17.8 (s, 1H) 15

δ (ppm) = 0.95 (t, 3H), 1.25-1.60 (m, 16H), 1.75 (m, 2H), 2.50 (s, 3H), 4.20 (m, 2H), 6.80 (d, 1H), 7.30 (d, 1H), 17.8 (s, 1H) 16

δ (ppm) = 1.15 (s, 6H), 1.35 (t, 3H), 2.35 (s, 2H), 2.50 (s, 3H), 2.70 (s, 2H), 4.30 (m, 2H), 6.85 (d, 1H), 7.30 (d, 2 1H), 17.8 (s, 1H) 17

m.p. 155° C.-157° C. 18

m.p. 198° C.-200° C. 19

m.p. 122° C.-123° C. 20

δ (ppm) = 1.35 (t, 3H), 1.85-2.45 (m, 6H), 3.15 (m, 1H), 3.70 (m, 1H), 4.30 (m, 2H), 6.35 (s, 1H), 7.15 (m, 2H), 7.60 (s, 1H), 7.85 (s, 1H) 21

m.p. 150° C.-151° C. 22

δ (ppm) = 1.00 (t, 3H), 1.35 (s, 6H), 1.55 (s, 6H), 1.75 (m, 2H), 2.50 (s, 3H), 4.15 (m, 2H), 6.85 (d, 1H), 7.25 (d, 1H), 18.0 (s, 1H) 23

m.p. 160° C.-162° C. 24

m.p. 158° C.-162° C. 25

m.p. 129° C.-135° C. 26

m.p. 135° C.-144° C. 27

δ (ppm) = 1.75 (m, 2H), 1.95-2.30 (m, 2H), 2.45 (s, 3H), 2.90 (m, 1H), 3.15 (m, 1H), 3.80-4.00 (m, 4H), 4.35 (m, 2H), 5.00 (m, 1H), 6.85 (d, 1H), 7.30 (d, 1H), 17.6 (s, 1H) 28

δ (ppm) = 1.35 (t, 3H), 1.50 (s, 6H), 1.60 (s, 6H), 2.65 (s, 3H), 4.25 (m, 2H), 6.30 (s, 1H), 7.20 (d, 1H), 7.30 (d, 1H), 7.50-7.60 (m, 2H) 29

m.p. 189° C.-193° C. 30

δ (ppm) = 1.00 (t, 3H), 1.35 (s, 6H), 1.55 (s, 6H), 1.80 (m, 2H), 2.45 (s, 3H), 3.95 (m, 2H), 6.80 (d, 1H), 7.10 (d, 1H), 17.8 (s, 1H) 31

δ (ppm) = 0.90 (t, 3H), 1.25-1.60 (m, 16H), 1.75 (m, 2H), 2.50 (s, 3H), 4.00 (m, 2H), 5.30, (s, 2H), 6.85 (d, 1H), 7.10 (d, 1H), 17.6 (s, 1H) 32

m.p. 161° C.-166° C. 33

m.p. 147° C.-149° C. 34

δ (ppm) = 0.90 (t, 3H), 1.25-1.80 (m, 18H), 2.50 (s, 3H), 4.20 (m, 2H), 6.85 (d, 1H), 7.30 (d, 1H), 18.0 (s, 1H) 35

δ (ppm) = 0.90 (t, 3H), 1.35-2.25 (m, 12H), 2.90 (m, 1H), 3.15 (m, 1H), 4.15 (m, 2H), 6.85 (d, 1H), 7.30 (d, 1H), 18.0 (s, 1H) 36

δ (ppm) = 0.90 (t, 3H), 1.15 (s, 6H), 1.50-1.80 (m, 6H), 2.30, (s, 2H), 2.40 (s, 3H), 2.70 (s, 2H), 4.00 (m, 2H), 6.80 (d, 1H), 7.10 (d, 1H), 17.8 (s, 1H) 37

δ (ppm) = 1.65-2.10 (m, 10H), 2.90 (m, 1H), 3.20 (m, 1H), 4.20 (m, 1H), 5.05 (m, 2H), 5.80 (m, 2H), 6.85 (d, 1H), 7.30 (d, 1H), 17.8 (s, 1H) 38

δ (ppm) = 1.25 (s, 6H), 1.50 (s, 6H), 2.30 (s, 3H), 3.75 (s, 3H), 5.45 (s, 2H), 6.60 (s, 1H), 6.65 (d, 1H), 6.75 (d, 1H), 6.85 (d, 1H), 7.25 (d, 1H), 7.35 (d, 1H), 17.8 (s, 1H) 39

δ (ppm) = 1.30-1.65 (m, 12H), 2.45 (m, 2H), 2.50 (s, 3H), 4.25 (m, 2H), 5.05-5.15 (m, 2H), 5.85 (m, 1H), 6.85 (d, 1H), 7.30 (d, 1H), 17.8 (s, 1H) 40

m.p. 129° C.-132° C.

The compounds I and their agriculturally useful salts are suitable, both as isomer mixtures and in the form of the pure isomers, for use as herbicides. The herbicidal compositions comprising compounds I effect very good control of vegetation on non-crop areas, especially at high application rates. In crops such as wheat, rice, maize, soybeans and cotton, they act against broad-leaved weeds and grass weeds without causing any significant damage to the crop plants. This effect is observed in particular at low application rates.

Depending on the application method in question, the compounds I or the herbicidal compositions comprising them can additionally be employed in a further number of crop plants for eliminating undesirable plants. Suitable crops are, for example, the following:

Allium cepa, Ananas comosus, Arachis hypogaea, Asparagus officinalis, Beta vulgaris spec. altissima, Beta vulgaris spec. rapa, Brassica napus var. napus, Brassica napus var. napobrassica, Brassica rapa var. silvestris, Camellia sinensis, Carthamus tinctorius, Carya illinoinensis, Citrus limon, Citrus sinensis, Coffea arabica (Coffea canephora, Coffea liberica), Cucumis sativus, Cynodon dactylon, Daucus carota, Elaeis guineensis, Fragaria vesca, Glycine max, Gossypium hirsutum, (Gossypium arboreum, Gossypium herbaceum, Gossypium vitifolium), Helianthus annuus, Hevea brasiliensis, Hordeum vulgare, Humulus lupulus, Ipomoea batatas, Juglans regia, Lens culinaris, Linum usitatissimum, Lycopersicon lycopersicum, Malus spec., Manihot esculenta, Medicago sativa, Musa spec., Nicotiana tabacum (N.rustica), Olea europaea, Oryza sativa, Phaseolus lunatus, Phaseolus vulgaris, Picea abies, Pinus spec., Pisum sativum, Prunus avium, Prunus persica, Pyrus communis, Ribes sylvestre, Ricinus communis, Saccharum officinarum, Secale cereale, Solanum tuberosum, Sorghum bicolor (s. vulgare), Theobroma cacao, Trifolium pratense, Triticum aestivum, Triticum durum, Vicia faba, Vitis vinifera and Zea mays.

In addition, the compounds I can also be used in crops which tolerate the action of herbicides due to breeding, including genetic engineering methods.

The compounds I, or the compositions comprising them, can be applied, for example, in the form of directly sprayable aqueous solutions, powders, suspensions, including highly-concentrated aqueous, oily or other suspensions or dispersions, emulsions, oil dispersions, pastes, dusts, mat rials for broadcasting or granules, by means of spraying, atomizing, dusting, broadcasting, pouring or seed dressing or mixing with the seed. The use forms depend on the intended purposes; in each case, they should ensure the finest possible distribution of the active compounds according to the invention. The herbicidal compositions comprise a herbicidally effective amount of at least one compound of the formula I or an agriculturally useful salt of I and auxiliaries which are customarily used for formulating crop protection agents.

Suitable inert additives are essentially:

-   -   Mineral oil fractions of medium to high boiling point, such as         kerosene and diesel oil, furthermore coal tar oils and oils of         vegetable or animal origin, aliphatic, cyclic and aromatic         hydrocarbons, for example paraffin, tetrahydro-naphthalene,         alkylated naphthalenes and their derivatives, alkylated benzenes         and their derivatives, alcohols such as methanol, ethanol,         propanol, butanol and cyclohexanol, ketones such as         cyclohexanone, strongly polar solvents, for example amines such         as N-methylpyrrolidone, and water.

Aqueous use forms can be prepared from emulsion concentrates, suspensions, pastes, wettable powders or water-dispersible granules by adding water. To prepare emulsions, pastes or oil dispersions, the compounds of the formula I, as such or dissolved in an oil or solvent, can be homogenized in water by means of wetting agent, tackifier, dispersant or emulsifier.

Alternatively, it is possible to prepare concentrates from active substance, wetting agent, tackifier, dispersant or emulsifier and, if desired, solvent or oil, and these concentrates are suitable for dilution with water.

Suitable surfactants are the alkali metal salts, alkaline earth metal salts and ammonium salts of aromatic sulfonic acids, for example ligno-, phenol-, naphthalene- and dibutylnaphthalene-sulfonic acid, and of fatty acids, of alkyl- and alkylaryl-sulfonates, of alkyl sulfates, lauryl ether sulfates and fatty alcohol sulfates, and the salts of sulfated hexa-, hepta- and octadecanols and of fatty alcohol glycol ethers, condensates of sulfonated naphthalene and its derivatives with formaldehyde, condensates of naphthalene or of the naphthalenesulfonic acids with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctyl-, octyl- or nonylphenol, alkylphenyl polyglycol ethers, tributylphenyl polyglycol ether, alkylaryl polyether alcohols, isotridecyl alcohol, fatty alcohol/ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers or polyoxypropylene alkyl ethers, lauryl alcohol polyglycol ether acetate, sorbitol esters, lignin-sulfite waste liquors or methylcellulose.

Powders, materials for spreading and dusts can be prepared by mixing or concomitant grinding of the active substances with a solid carrier.

Granules, e.g. coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active compounds to solid carriers. Solid carriers are mineral earths such as silicas, silica gels, silicates, talc, kaolin, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders, or other solid carriers.

The concentrations of the active compounds I in the ready-to-use products can be varied within wide ranges. In general, the formulations comprise from 0.001 to 98% by weight, preferably 0.01 to 95% by weight, of at least one active compound. The active compounds are employed in a purity of from 90% to 100%, preferably 95% to 100% (according to NMR spectrum).

The compounds I according to the invention can be formulated, for example, as follows:

-   I. 20 parts by weight of the compound of the formula I are dissolved     in a mixture composed of 80 parts by weight of alkylated benzene, 10     parts by weight of the adduct of 8 to 10 mol of ethylene oxide to 1     mol of oleic acid N-monoethanolamide, 5 parts by weight of calcium     dodecylbenzenesulfonate and 5 parts by weight of the adduct of 40     mol of ethylene oxide and 1 mol of castor oil. Pouring the solution     into 100,000 parts by weight of water and finely distributing it     therein gives an aqueous dispersion which comprises 0.02% by weight     of the active compound. -   II. 20 parts by weight of the compound of the formula I are     dissolved in a mixture composed of 40 parts by weight of     cyclohexanone, 30 parts by weight of isobutanol, 20 parts by weight     of the adduct of 7 mol of ethylene oxide to 1 mol of isooctylphenol     and 10 parts by weight of the adduct of 40 mol of ethylene oxide to     1 mol of castor oil. Pouring the solution into 100,000 parts by     weight of water and finely distributing it therein gives an aqueous     dispersion which comprises 0.02% by weight of the active compound. -   III. 20 parts by weight of the active compound of the formula I are     dissolved in a mixture composed of 25 parts by weight of     cyclohexanone, 65 parts by weight of a mineral oil fraction of     boiling point 210 to 280° C. and 10 parts by weight of the adduct of     40 mol of ethylene oxide and 1 mol of castor oil. Pouring the     solution into 100,000 parts by weight of water and finely     distributing it therein gives an aqueous dispersion which comprises     0.02% by weight of the active compound. -   IV. 20 parts by weight of the active compound of the formula I are     mixed thoroughly with 3 parts by weight of sodium     diisobutylnaphthalenesulfonate, 17 parts by weight of the sodium     salt of a lignosulfonic acid from a sulfite waste liquor and 60     parts by weight of pulverulent silica gel, and the mixture is ground     in a hammer mill. Finely distributing the mixture in 20,000 parts by     weight of water gives a spray mixture which comprises 0.1% by weight     of the active compound. -   V. 3 parts by weight of the active compound of the formula I are     mixed with 97 parts by weight of finely divided kaolin. This gives a     dust which comprises 3% by weight of the active compound. -   VI. 20 parts by weight of the active compound of the formula I are     mixed intimately with 2 parts by weight of calcium     dodecylbenzenesulfonate, 8 parts by weight of fatty alcohol     polyglycol ether, 2 parts by weight of the sodium salt of a     phenol/urea/formaldehyde condensate and 68 parts by weight of a     paraffinic mineral oil. This gives a stable oily dispersion. -   VII. 1 part by weight of the compound of the formula I is dissolved     in a mixture composed of 70 parts by weight of cyclohexanone, 20     parts by weight of ethoxylated isooctylphenol and 10 parts by weight     of ethoxylated castor oil. This gives a stable emulsion concentrate. -   VIII. 1 part by weight of the compound of the formula I is dissolved     in a mixture composed of 80 parts by weight of cyclohexanone and 20     parts by weight of Wettol® EM 31 (=non-ionic emulsifier based on     ethoxylated castor oil). This gives a stable emulsion concentrate.

The herbicidal compositions or the active compounds can be applied pre- or post-emergence or together in the seed of a crop plant. It is also possible to apply the herbicidal compositions or active compounds by applying crop plant seed pretreated with the herbicidal compositions or active compounds. If the active compounds are less well tolerated by certain crop plants, it is possible to use application techniques in which the herbicidal compositions are sprayed, with the aid of the spraying equipment, in such a way that they come into as little contact as possible, if any, with the leaves of the sensitive crop plants while the active compounds reach the leaves of undesirable plants which grow underneath, or the bare soil surface (post-directed, lay-by).

Depending on the intended aim, the season, the target plants and the growth stage, the rates of application of the active compound I are from 0.001 to 3.0, preferably 0.01 to 1.0, kg of active substance (a.s.)/ha.

To widen the spectrum of action and to achieve synergistic effects, the novel compounds of the formula I may be mixed, and applied jointly, with a large number of representatives of other groups of herbicidally or growth-regulating active compounds. Suitable examples of components in mixtures are 1,2,4-thiadiazoles, 1,3,4-thiadiazoles, amides, aminophosphoric acid and its derivatives, aminotriazoles, anilides, (het)aryloxyalkanoic acids and their derivatives, benzoic acid and its derivatives, benzothiadiazinones, 2-aroyl-1,3-cyclohexanediones, 2-hetaroyl-1,3-cyclohexanedione, hetaryl aryl ketones, benzylisoxazolidinones, meta-CF₃-phenyl derivatives, carbamates, quinolinecarboxylic acid and its derivatives, chloroacetanilides, cyclohexenone oxime ether derivatives, diazines, dichloropropionic acid and its derivatives, dihydrobenzofurans, dihydrofuran-3-ones, dinitroanilines, dinitrophenols, diphenyl ethers, dipyridyls, halocarboxylic acids and their derivatives, ureas, 3-phenyluracils, imidazoles, imidazolinones, N-phenyl-3,4,5,6-tetrahydrophthalimides, oxadiazoles, oxiranes, phenols, aryloxy- and hetaryloxyphenoxypropionic esters, phenylacetic acid and its derivatives, phenylpropionic acid and its derivatives, pyrazoles, phenylpyrazoles, pyridazines, pyridinecarboxylic acid and its derivatives, pyrimidyl ethers, sulfonamides, sulfonylureas, triazines, triazinones, triazolinones, triazolecarboxamides and uracils.

Moreover, it may be advantageous to apply the compounds I alone or in combination with other herbicides, even in the form of a mixture together with further crop protection agents, for example with pesticides or agents for controlling phytopathogenic fungi or bacteria. Also of interest is the miscibility with mineral salt solutions which are employed for treating nutritional and trace element deficiencies. Nonphytotoxic oils and oil concentrates may also be added.

USE EXAMPLES

The herbicidal activity of the cyclohexenone derivatives of benzazolones of the formula I was demonstrated by the following greenhouse experiments:

The culture containers used were plastic pots containing loamy sand with approximately 3.0% of humus as substrate. The seeds of the test plants were sown separately for each species.

For the pre-emergence treatment, the active compounds, suspended or emulsified in water, were applied directly after sowing by means of finely distributing nozzles. The containers were irrigated gently to promote germination and growth and subsequently covered with translucent plastic hoods until the plants had rooted. This cover caused uniform germination of the test plants unless this was adversely affected by the active compounds.

For the post-emergence treatment, the test plants were first grown to a plant height of from 3 to 15 cm, depending on the plant habit, and only then treated with the active compounds which had been suspended or emulsified in water. To this end, the test plants were either sown directly and grown in the same containers, or they were first grown separately as seedlings and transplanted into the test containers a few days prior to treatment. The rate of application for the post-emergence treatment was 250, 125, 62.5, 31.3 and/or 15.6 g/ha of active substance (a.s.).

Depending on the species, the plants were kept at from 10 to 25° C., or 20-35° C., respectively. The test period extended over 2 to 4 weeks. During this time, the plants were tended, and their response to the individual treatments was evaluated.

Evaluation was carried out using a scale of from 0 to 100. 100 means no emergence of the plants, or complete destruction of at least the aerial parts, and 0 means no damage, or normal course of growth. A damage of at least 95% corresponds to very good herbicidal action.

The plants used in the greenhouse experiments were of the following species:

Bayer code Common name ABUTH velvet leaf AMARE redroot pigweed BRAPL marmalade grass CHEAL lambs' quarters (goose- foot) ECHCG barnyard grass LAMAM henbit MATIN chamomile, false PHBPU morning glory, common POLPE lady's thumb SINAL white mustard SETFA giant foxtail

The following results were obtained by the post-emergence method. At application rates of 125 or 62.5 g/ha (a.s.), the compound I-1a.1129 from Example 1, used by the post-emergence method, showed very good herbicidal action against CHEAL, LAMAM, MATIN and SINAL.

At application rates of 125 or 62.5 g/ha (a.s.), the compound I-1c.1129 from Example 2, used by the post-emergence method, showed very good herbicidal action against CHEAL, ECHCG, PHBPU und POLPE.

At application rates of 31.3 g/ha (a.s.), the compound I-1d.1129 from Example 3, used by the post-emergence method, showed very good herbicidal action against CHEAL, PHBPU and POLPE, good to very good herbicidal action against ECHCG and, at application rates of 16.5 g/ha of a.s., very good herbicidal action against PHBPU and POLPE and good to very good herbicidal action against CHEAL and ECHCG.

At application rates of 125 or 250 g/ha (a.s.), the compound I-1c.1131 from Example 16, used by the post-emergence method, showed very good herbicidal action against CHEAL, ECHCG, SETFA and POLPE.

At application rates of 125 or 250 g/ha (a.s.) the compound I-1x.1131 from Example 17, used by the post-emergence method, showed very good herbicidal action against BRAPL, CHEAL, ECHCG, SETFA and POLPE.

At application rates of 125 or 250 g/ha (a.s.) the compound I-1a.1131 from Example 18, used by the post-emergence method, showed very good herbicidal action against ABUTH, CHEAL, ECHCG and POLPE.

At application rates of 125 or 250 g/ha (a.s.) the compound I-1d.1131 from Example 19, used by the post-emergence method, showed very good herbicidal action against ABUTH, AMARE, CHEAL, ECHCG and SETFA.

At application rates of 125 or 250 g/ha (a.s.) the compound I-1x.1134 from Example 14, used by the post-emergence method, showed very good herbicidal action against ABUTH, CHEAL, ECHCG and SETFA.

At application rates of 125 or 250 g/ha (a.s.) the compound I-1d.1134 from Example 15, used by the post-emergence method, showed very good herbicidal action against ABUTH, AMARE, ECHCG and POLPE.

At application rates of 125 or 250 g/ha (a.s.) the compound I-1a.6 from Example 9, used by the post-emergence method, showed very good herbicidal action against AMARE, CHEAL, ECHCG and POLPE.

At application rates of 125 or 250 g/ha (a.s.) the compound I-1a.29 from Example 11, used by the post-emergence method, showed very good herbicidal action against AMARE, CHEAL, ECHCG and POLPE. 

1. A cyclohexenone derivative of a benzazolone of the formula I

in which A, R¹, R², R³ and Hex are as defined below: A is O, S, SO, SO₂ or NR⁶; R¹ is halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-hydroxyalkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₁-C₄-haloalkylthio-C₁-C₄-alkyl, C₁-C₄-alkylthio-C₁-C₄-alkyl, C₁-C₄-alkylsulfonyl-C₁-C₄-alkyl, C₁-C₄-haloalkylsulfonyl-C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-hydroxyalkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkoxy-C₁-C₄-alkoxy, C₁-C₄-haloalkoxy-C₁-C₄-alkoxy, C₁-C₄-alkylthio, C₁-C₄-haloalkylthio, C₁-C₄-alkylsulfonyl, C₁-C₄-haloalkylsulfonyl; R² is hydroxyl, nitro, amino, C₁-C₆-alkylamino, di(C₁-C₆-alkyl)amino, cyno, CHO, C₁-C₆-alkoxy, C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl, C₁-C₆-haloalkoxy-C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkeny, C₁-C₆-haloalkoxy-C₂-C₆-alkenyl, C₁-C₆-alkoxy-C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₁-C₆-haloalkoxy-C₂-C₆-alkynyl, C₁-C₆-alkoxy-C₂-C₆-alkynyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl, (C₁-C₆-alkyl)carbonyl, C₁-C₆-haloalkylcarbonyl, hydroxycarbonyl-C₁-C₄-alkyl, C₁-C₆-alkoxycarbonyl-C₁-C₆-alkyl, a radical of the formula C(O)OR⁴, CON(R⁵)₂ or C(═NOR^(4a))R^(4b), aryl, aryl-C₁-C₄-alkyl, arylsulfonyl, arylcarbonyl, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl, 3-, 4-, 5-, 6- or 7-membered heterocyclyl, 3-, 4-, 5-, 6- or 7-membered heterocyclyl-C₁-C₆-alkyl, where each aryl, cycloalkyl, cycloalkenyl and each heterocyclyl radical may be unsubstituted or may carry one, two, three or four substituents, in each case selected from the group consisting of halogen, C₁-C₄-haloalky, C₁-C₄-alkoxy and C₁-C₄-haloalkoxy; R³ is hydrogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-haloalkoxy-C₁-C₄-alkyl or halogen; in which R⁴ is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl, C₁-C₆-haloalkoxy-C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₁-C₆-haloalkoxy-C₂-C₆-alkenyl, C₁-C₆-alkoxy-C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₁-C₆-haloalkoxy-C₂-C₆-alkynyl, C₁-C₆-alkoxy-C₂-C₆-alkynyl; R^(4a), R^(4b) independently of one another may have the meanings mentioned for R⁴, and R^(4b) may be hydrogen; R⁵ independently of one another are hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy-C₁-C₆-alkyl, (C₁-C₆-haloalkoxy)-C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₁-C₆-haloalkyl-C₂-C₆-alkenyl, C₁-C₆-haloalkoxy-C₂-C₆-alkenyl, C₁-C₆-alkoxy-C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₁-C₆-haloalkyl-C₂-C₆-alkynyl, C₁-C₆-haloalkoxy-C₂-C₆-alkynyl, C₁-C₆-alkoxy-C₂-C₆-alkynyl, or together form a 3- to 7-membered heterocycle which may be partially or fully halogenated and/or may carry one, two or three substituents selected from the group consisting of C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy; R⁶ is hydrogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl; and Hex is substituted (3-oxo-1-cyclohexen-2-yl)carbonyl of the formula IIa or substituted (1,3-dioxo-2-cyclohexyl)methylidene of the formula IIb,

in which the variables R⁷ to R¹³ are as defined below: R⁷ is hydroxyl, mercapto, halogen, OR¹⁴, SR¹⁴, SOR¹⁵, SO₂R¹⁵, OSO₂R¹⁵, P(O)R¹⁶R¹⁷, OP(O)R¹⁶R¹⁷, P(S)R¹⁶R¹⁷, OP(S)R¹⁶R¹⁷, NR¹⁸R¹⁹, ONR¹⁸R¹⁹ or N-bonded heterocyclyl which may be partially or fully halogenated an for may carry one to three of the following radicals: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy; R⁸, R¹² independently of one another are hydrogen, C₁-C₄-alkyl or C₁-C₄-alkoxycarbonyl; R^(9,)R¹¹R¹³ independently of one another are hydrogen or C₁-C₄-alkyl; R¹⁰ is hydrogen, halogen, hydroxyl, C₁-C₆-alkyl, C₁-C₆-haloalkyl, di-(C₁-C₆-alkoxy)-methyl,(C₁-C₆-alkoxy)-(C₁-C₆-alkylthio)methyl, di-(C₁-C₆-alkylthio)methyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkylthio, C₁-C₆-haloalkylthio, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl, C₁-C₆-alkoxycarbonyl, C₁-C₆-haloalkoxycarbonyl; is 1,3-dioxolan-2-yl, 1,3-dioxan-2-yl, 1,3-oxathiolan-2-yl, 1,3-oxathian-2-yl, 1,3-dithiolan-2-yl or 1,3-dithian-2-yl, where the six lastmentioned radicals may be substituted by one to three C₁-C₄-alkyl radicals; or R⁹ and R¹¹ or R¹¹ and R¹³ together form a π bond or a C₁-C₅-alkylene chain which may carry one, two or three radicals from the following group: halogen, cyano, 1-C₄-alkyl, C₁-C₄-haloalkyl or C₁-C₄-alkoxycarbonyl; or R⁹ and R¹³ together form a C₁-C₄-alkyl chain which may carry one, two or three radicals from the following group: halogen, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl or C₁-C₄-alkoxycarbonyl; or R¹⁰ and R¹¹ together form a —O—CH₂)_(p)—O—, —O—(CH₂)_(p)—S—, —S—(CH₂)_(p)—S—, —O—(CH₂)_(q)— or —S—(CH₂)_(q)— chain, in which p is 2, 3, 4 or 5 and q is 2, 3, 4, 5 or 6, which may substituted by one, two or three radicals frclm the following group: halogen, cyano, C₁-C₄-alkyl, C₁-C₁-C₄-haloalkyl or C₁-C₄-alkoxycarbonyl; or R¹⁰ and R¹¹, together with the carbon to which they are attached, form a carbonyl group; where R¹⁴ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-alkynyl, C₃-C₆-haloalkynyl, C₃-C₆-cycloalkyl, C₁-C₆-alkylcarbonyl, C₂-C₆-alkenylcarbonyl, C₂-C₆-alkynylcarbonyl, C₃-C₆-cycloalkylcarbonyl, C₁-C₆-alkoxycarbonyl, C₃-C₆-alkenyloxycarbonyl, C₃-C₆-alkynyloxycarbonyl, C₁-C₆-alkylthiocarbonyl, C₁-C₆-alkylaminocarbonyl, C₃-C₆-alkenylaminocarbonyl, C₃-C₆-alkynylaminocarbonyl, N,N-di(C₁-C₆-alkyl)amino-carbonyl, N-(C₃-C₆-alkenyl)-N-(C₁-C₆-alkyl)amino-carbonyl, N-(C₃-C₆-alkynyl)-N-(C₁-C₆-alkyl)amino-carbonyl, N-(C₁-C₆-alkoxy)-N-(C₁-C₆-alkyl)amino-carbonyl, N-(C₃-C₆-alkenyl)-N-(C₁-C₆-alkoxy)amino-carbonyl, N-(C₃-C₆-alkynyl)-N-(C₁-C₆-alkoxy)amino-carbonyl, di(C₁-C₆-alkyl)aminothiocarbonyl, C₁-C₆-alkoxyimino-C₁-C₆-alkyl, where the alkyl, cycloalkyl and alkoxy radicals mentioned may be partially or fully halogenated and/or may carry one, two or three of the following groups: cyano, C₁-C₄-alkoxy, C₁-C₄-alkylthio, di(C₁-C₄-alkyl)amino, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, C₁-C₄-alkoxy-C₁-C₄-alkoxycarbonyl, hydroxycarbonyl, C₁-C₄-alkylaminocarbonyl, di(C₁-C₄-alkyl)amino-carbonyl, aminocarbonyl, C₁-C₄-alkylcarbonyloxyor C₃-C₆-cycloalkyl; is phenyl, phenyl-C₁-C₆-alkyl, phenylcarbonyl-C₁-C₆-alkyl, phenylcarbonyl, phenoxycarbonyl, phenoxythiocarbonyl, phenylaminocarbonyl, N-(C₁-C₆-alkyl)-N-phenylaminocarbonyl, phenyl-C₂-C₆-alkenylcarbonyl, heterocyclyl, heterocyclyl-C₁-C₆-alkyl, heterocyclylcarbonyl-C₁-C₆-alkyl, heterocyclylcarbonyl, heterocyclyloxycarbonyl, heterocyclyloxythiocarbonyl, heterocyclylamino-carbonyl, N-(C₁-C₆alkyl)-N-heterocyclyl-aminocarbonyl, or heterocyclyl-C₁-C₆-alkenylcarbonyl, where the phenyl and the heterocyclyl radical of the 18 lastmentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy; R¹⁵ is C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-alkynyl or C₃-C₆-cycloalkyl, where the four radicals mentioned may be partially or fully halogenated and/or may carry one, two or three of the following groups: cyano, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylthio, C₁-C₄-haloalkylthio, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl or C₁-C₄-haloalkoxycarbonyl; is phenyl, phenyl-C₁-C₄-alkyl, heterocyclyl or heterocyclyl-C₁-C₄-alkyl, where the phenyl and the heterocyclyl radical of the four lastmentioned substituents may be partially or fully halogenated and/or may carry one, two or three of the following radicals: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl; R¹⁶, R¹⁷ independently of one another are hydrogen, hydroxyl, C₁-C₆alkyl, C₁-C₆-alkoxy, C₁-C₆-alkylthio, phenyl, phenyl-C₁-C₄-alkyl or phenoxy, where the three lastmentioned substituents may be partially or fully halogenated and/or may carry one, two or three of the following radicals: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy or C₁-C₄-alkoxycarbonyl; R¹⁸ is hydrogen, C₁-C₆-alkyl, C₃-C₆-alkenyl, C₃-C₆-haloalkenyl, C₃-C₆-alkynyl, C₃-C₆-haloalkynyl, C₃-C₆-cycloalkyl, C₁-C₆-alkylcarbonyl, hydroxyl, C₁-C₆-alkoxy, C₃-C₆-alkenyloxy, C₃-C₆-alkynyloxy, amino, C₁-C₆-alkylamino, di(C₁-C₆-alkyl)amino or C₁-C₆-alkylcarbonylamino, where the alkyl, cycloalkyl or alkoxy radicals mentioned may be partially or fully halogenated and/or may carry one, two or three of the following radicals: cyano, C₁-C₄-alkoxy-carbonyl, C₁-C₄-alkylaminocarbonyl, di(C₁-C₄-alkyl)-aminocarbonyl or C₃-C₆-cycloalkyl; is phenyl, phenyl-C₁-C₄-alkyl, phenylcarbonyl, heterocyclyl, heterocyclyl-C₁-C₄-alkyl or heterocyclylcarbonyl, where the phenyl or heterocyclyl radical of the six lastmentioned substituents may be partially or fully halogenated and/or may carry one to three of the following radicals: nitro, cyano, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy or C₁-C₄-haloalkoxy; R¹⁹ is hydrogen, C₁-C₆-alkyl, C₃-C₆-alkenyl or C₃-C₆-alkynyl; and its agriculturally useful salts.
 2. A cyclohexenone derivative as claimed in claim 1 wherein A in the formula I is oxygen or NR⁶.
 3. A cyclohexenone derivative as claimed in claim 1 wherein A in the formula I is sulfur.
 4. A cyclohexenone derivative as claimed in claim 1 where R¹ in the formula I is selected from the group consisting of C₁-C₄-alkyl, halogen and C₁-C₄-alkoxy.
 5. A cyclohexenone derivative as claimed in claim 1 where R² in the formula I is a heterocycle selected from the group consisting of 4,5-dihydroisoxazol-3-yl, 4,5-dihydroisoxazol-4-yl, isoxazol-3-yl, isoxazol-4-yl, 1,3-dioxolan-2-yl, 1,3-dithiolan-2-yl, 1,3-dioxan-2-yl, 1,3-dithian-2-yl, oxazolin-2-yl and oxazolidin-2-yl, where the abovementioned heterocycles may be mono-, di- or trisubstituted by C₁-C₄-alkyl.
 6. A cyclohexenone derivative as claimed in claim 1, where R² in the formula I is cyano, C₁-C₄-alkyl, C₃-C₆-alkenyl, C₁-C₄-(halo)alkylcarbonyl, C₁-C₄-alkoxycarbonyl-C₁-C₄-alkyl or C₁-C₄-alkoxycarbonyl.
 7. A cyclohexenone derivative as claimed in claim 1 where R³ in the formula I is hydrogen, C₁-C₄-alkyl or halogen.
 8. A cyclohexenone derivative as claimed in claim 1 where Hex in the formula I is a radical of the formula IIa where R⁷ is selected from the group consisting of hydroxyl, mercapto, halgen, OR¹⁴, SR¹⁴, SO₂R¹⁵, NR¹⁸R¹⁹ and ONR¹⁸R¹⁹, where R¹⁴, R¹⁵ and R¹⁹ are as defined in claim
 1. 9. A cyclohexenone derivative as claimed in claim 8 where in the formula IIa or IIb. R⁷ is selected from the group consisting of hydroxyl, C₁-C₄-alkyloxy, C₁-C₄-alkylamino, di-C₁-C₄-alkylamino, N-(C₁-C₄-alkyloxy)-N-(C₁-C₄-alkyl)amino, O—CH₂-phenyl, phenylthio, phenylcarbonyloxy, 2-, 3- or 4-fluorophenylcarbonyloxy, C₁-C₄-methylthio, C₁-C₄-sulfonyloxy, phenylsulfonyloxy and 2-, 3- or 4-ethylphenyl-sulfonyloxy.
 10. A cyc;ohexenone derivative as claimed in claim 1 where in the formula IIa or IIb R⁹, R⁹, R¹⁰, R¹¹, R¹² and R¹³ independently of one another are hydrogen or C₁-C₄-alkyl, R¹⁰ may also be hydroxyl, C₁-C₄-alkoxy, C₁-C₄-alkylthio, haloalkoxy or haloalkylthio, R¹⁰ and R¹¹ together with the carbon atom to which they are attached may also be a carbonyl group or a 1,3-dioxolane, 1,3-dithiolane, 1,3-oxothiolane, 1,3-oxothiane, 1,3-dithiolane or 1,3-dithiane ring, where the 2-position of the six rings mentioned is identical to the carbon to which R¹⁰ and R¹¹ are attached, R⁸ and R¹² or R⁹ and R¹³ may also be a C₁-C₄-alkylene chain, or R⁹ and R¹¹ or R¹¹ and R¹² together may form a π bond.
 11. A benzazolonecarboxylic acid of the formula IVa

where A, R¹, R² and R³ are defined in claim
 1. 12. A composition, comprising at least one cyclohexenone derivative of the formula I or an agriculturally useful salt of I as claimed in claim 1, and custormay auxiliaries.
 13. A method for controlling undesirable vegetation, which comprises allowing a herbicidally effective amount of at least one cyclohexenone derivative of the formula I or an agriculturally useful salt of I as claimed in claim 1 to act on plants, their habitat and/or on seed. 